2124-47-2|2,4-Dimethyl-5-nitroaniline| Ambeed

CAS No. :	2124-47-2
Formula :	C₈H₁₀N₂O₂
M.W :	166.18
SMILES Code :	NC1=CC([N+]([O-])=O)=C(C)C=C1C
MDL No. :	MFCD00025199
InChI Key :	DUIOVGPUAJSYCD-UHFFFAOYSA-N
Pubchem ID :	228007

Safety of [ 2124-47-2 ]

GHS Pictogram:
Signal Word:	Warning
Hazard Statements:	H302
Precautionary Statements:	P280-P305+P351+P338

Computational Chemistry of [ 2124-47-2 ] Show Less

Physicochemical Properties

Num. heavy atoms	12
Num. arom. heavy atoms	6
Fraction Csp3	0.25
Num. rotatable bonds	1
Num. H-bond acceptors	2.0
Num. H-bond donors	1.0
Molar Refractivity	49.6
TPSA ? Topological Polar Surface Area: Calculated from Ertl P. et al. 2000 J. Med. Chem.	71.84 Å²

Lipophilicity

Log P_o/w (iLOGP)? iLOGP: in-house physics-based method implemented from Daina A et al. 2014 J. Chem. Inf. Model.	1.42
Log P_o/w (XLOGP3)? XLOGP3: Atomistic and knowledge-based method calculated by XLOGP program, version 3.2.2, courtesy of CCBG, Shanghai Institute of Organic Chemistry	1.8
Log P_o/w (WLOGP)? WLOGP: Atomistic method implemented from Wildman SA and Crippen GM. 1999 J. Chem. Inf. Model.	1.8
Log P_o/w (MLOGP)? MLOGP: Topological method implemented from Moriguchi I. et al. 1992 Chem. Pharm. Bull. Moriguchi I. et al. 1994 Chem. Pharm. Bull. Lipinski PA. et al. 2001 Adv. Drug. Deliv. Rev.	0.94
Log P_o/w (SILICOS-IT)? SILICOS-IT: Hybrid fragmental/topological method calculated by FILTER-IT program, version 1.0.2, courtesy of SILICOS-IT, http://www.silicos-it.com	-0.14
Consensus Log P_o/w? Consensus Log P_o/w: Average of all five predictions	1.17

Water Solubility

Log S (ESOL):? ESOL: Topological method implemented from Delaney JS. 2004 J. Chem. Inf. Model.	-2.31
Solubility	0.817 mg/ml ; 0.00492 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Soluble
Log S (Ali)? Ali: Topological method implemented from Ali J. et al. 2012 J. Chem. Inf. Model.	-2.93
Solubility	0.196 mg/ml ; 0.00118 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Soluble
Log S (SILICOS-IT)? SILICOS-IT: Fragmental method calculated by FILTER-IT program, version 1.0.2, courtesy of SILICOS-IT, http://www.silicos-it.com	-2.19
Solubility	1.08 mg/ml ; 0.00652 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Soluble

Pharmacokinetics

GI absorption? Gatrointestinal absorption: according to the white of the BOILED-Egg	High
BBB permeant? BBB permeation: according to the yolk of the BOILED-Egg	Yes
P-gp substrate? P-glycoprotein substrate: SVM model built on 1033 molecules (training set) and tested on 415 molecules (test set) 10-fold CV: ACC=0.72 / AUC=0.77 External: ACC=0.88 / AUC=0.94	No
CYP1A2 inhibitor? Cytochrome P450 1A2 inhibitor: SVM model built on 9145 molecules (training set) and tested on 3000 molecules (test set) 10-fold CV: ACC=0.83 / AUC=0.90 External: ACC=0.84 / AUC=0.91	Yes
CYP2C19 inhibitor? Cytochrome P450 2C19 inhibitor: SVM model built on 9272 molecules (training set) and tested on 3000 molecules (test set) 10-fold CV: ACC=0.80 / AUC=0.86 External: ACC=0.80 / AUC=0.87	No
CYP2C9 inhibitor? Cytochrome P450 2C9 inhibitor: SVM model built on 5940 molecules (training set) and tested on 2075 molecules (test set) 10-fold CV: ACC=0.78 / AUC=0.85 External: ACC=0.71 / AUC=0.81	No
CYP2D6 inhibitor? Cytochrome P450 2D6 inhibitor: SVM model built on 3664 molecules (training set) and tested on 1068 molecules (test set) 10-fold CV: ACC=0.79 / AUC=0.85 External: ACC=0.81 / AUC=0.87	No
CYP3A4 inhibitor? Cytochrome P450 3A4 inhibitor: SVM model built on 7518 molecules (training set) and tested on 2579 molecules (test set) 10-fold CV: ACC=0.77 / AUC=0.85 External: ACC=0.78 / AUC=0.86	No
Log Kp (skin permeation)? Skin permeation: QSPR model implemented from Potts RO and Guy RH. 1992 Pharm. Res.	-6.04 cm/s

Druglikeness

Lipinski? Lipinski (Pfizer) filter: implemented from Lipinski CA. et al. 2001 Adv. Drug Deliv. Rev. MW ≤ 500 MLOGP ≤ 4.15 N or O ≤ 10 NH or OH ≤ 5	0.0
Ghose? Ghose filter: implemented from Ghose AK. et al. 1999 J. Comb. Chem. 160 ≤ MW ≤ 480 -0.4 ≤ WLOGP ≤ 5.6 40 ≤ MR ≤ 130 20 ≤ atoms ≤ 70	None
Veber? Veber (GSK) filter: implemented from Veber DF. et al. 2002 J. Med. Chem. Rotatable bonds ≤ 10 TPSA ≤ 140	0.0
Egan? Egan (Pharmacia) filter: implemented from Egan WJ. et al. 2000 J. Med. Chem. WLOGP ≤ 5.88 TPSA ≤ 131.6	0.0
Muegge? Muegge (Bayer) filter: implemented from Muegge I. et al. 2001 J. Med. Chem. 200 ≤ MW ≤ 600 -2 ≤ XLOGP ≤ 5 TPSA ≤ 150 Num. rings ≤ 7 Num. carbon > 4 Num. heteroatoms > 1 Num. rotatable bonds ≤ 15 H-bond acc. ≤ 10 H-bond don. ≤ 5	1.0
Bioavailability Score? Abbott Bioavailability Score: Probability of F > 10% in rat implemented from Martin YC. 2005 J. Med. Chem.	0.55

Medicinal Chemistry

PAINS? Pan Assay Interference Structures: implemented from Baell JB. & Holloway GA. 2010 J. Med. Chem.	0.0 alert
Brenk? Structural Alert: implemented from Brenk R. et al. 2008 ChemMedChem	3.0 alert: heavy_metal
Leadlikeness? Leadlikeness: implemented from Teague SJ. 1999 Angew. Chem. Int. Ed. 250 ≤ MW ≤ 350 XLOGP ≤ 3.5 Num. rotatable bonds ≤ 7	No; 1 violation:MW<1.0
Synthetic accessibility? Synthetic accessibility score: from 1 (very easy) to 10 (very difficult) based on 1024 fragmental contributions (FP2) modulated by size and complexity penaties, trained on 12'782'590 molecules and tested on 40 external molecules (r² = 0.94)	2.0

Application In Synthesis of [ 2124-47-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

Upstream synthesis route of [ 2124-47-2 ]
Downstream synthetic route of [ 2124-47-2 ]

[ 2124-47-2 ] Synthesis Path-Upstream 1~2

1
[ 2124-47-2 ]
[ 69383-68-2 ]

Yield	Reaction Conditions	Operation in experiment
47%	With sodium nitrite In hydrogenchloride; water	4-Chloro-6-nitro-m-xylene A solution of sodium nitrite (7.2 g, 0.1 mol) in water (20 mL) was added dropwise over 45 min at <5 °C to a stirred suspension of 5-nitro-2,4-xylidine (16.6 g, 0.1 mol) in conc. hydrochloric acid (300 mL). After complete addition the reaction was stirred at <5 °C for 1 h then a solution of copper(I)chloride (16.0 g, 0.16 mol) in conc. hydrochloric acid (50 mL) was added dropwise over 20 min at <5 °C (CARE: effervescence at first). The reaction was then warmed from 0 °C to room temperature and stirred for 18 h. The mixture was then carefully poured into water (1 L) and extracted with ethyl acetate (3 x 300 mL). The combined organic extracts were dried (magnesium sulfate), filtered and the solvent removed under vacuum to leave a crude oil. The oil was purified by flash column chromatography (SiO₂; heptane) to give the product as a yellow oil (8.8 g, 47percent). IR ν_max (film)/cm^-1 3103, 2985, 2935, 2863, 2744, 2432, 1610, 1572, 1518, 1480, 1454, 1384, 1346, 1286, 1266, 1244, 1197, 1166, 1157, 1107, 1036, 982, 894, 842, 759, 746, 725, 704, 646 and 602; NMR δ_H (400 MHz; CDCl₃) 8.01 (1H, s), 7.20 (1H, s), 2.56 (3H, s), 2.41 (3H, s).

References: [1] Patent: EP1147110, 2003, B1, .

2
[ 2124-47-2 ]
[ 69383-68-2 ]

References: [1] Justus Liebigs Annalen der Chemie, 1892, vol. 271, p. 17.
[2] Recueil des Travaux Chimiques des Pays-Bas, 1952, vol. 71, p. 1213,1218.

[ 2124-47-2 ] Synthesis Path-Downstream 1~54

1
[ 98-01-1 ]
[ 2124-47-2 ]
furfural-(2,4-dimethyl-5-nitro-phenylimine) [ No CAS ]

References: [1]Journal fur praktische Chemie (Leipzig 1954),1920,vol. <2> 100,p. 112.

2
[ 2124-47-2 ]
[ 4102-38-9 ]

References: [1]Bulletin of the Chemical Society of Japan,1965,vol. 38,p. 1590 - 1595.

3
[ 2124-47-2 ]
[ 3282-30-2 ]
[ 136539-29-2 ]

References: [1]Journal of Heterocyclic Chemistry,1991,vol. 28,p. 987 - 990.

4
[ 2124-47-2 ]
[ 186494-34-8 ]

References: [1]Journal of the American Chemical Society,1997,vol. 119,p. 6607 - 6613.
[2]Tetrahedron Letters,1996,vol. 37,p. 9207 - 9210.

5
[ 2124-47-2 ]
[ 186494-40-6 ]

References: [1]Journal of the American Chemical Society,1997,vol. 119,p. 6607 - 6613.
[2]Tetrahedron Letters,1996,vol. 37,p. 9207 - 9210.

6
[ 2124-47-2 ]
N,N,N',N'-Tetrakis-(4-methoxy-phenyl)-4,6-dimethyl-benzene-1,3-diamine [ No CAS ]

References: [1]Journal of the American Chemical Society,1997,vol. 119,p. 6607 - 6613.

7
[ 2124-47-2 ]
[ 186494-36-0 ]

References: [1]Tetrahedron Letters,1996,vol. 37,p. 9207 - 9210.

8
[ 2124-47-2 ]
[ 186494-35-9 ]

References: [1]Tetrahedron Letters,1996,vol. 37,p. 9207 - 9210.

9
[ 2124-47-2 ]
4,6-Dimethyl-N,N,N',N'-tetraphenyl-benzene-1,3-diamine [ No CAS ]

References: [1]Tetrahedron Letters,1996,vol. 37,p. 9207 - 9210.

10
[ 2124-47-2 ]
4,6-Dimethyl-N,N,N',N'-tetra-p-tolyl-benzene-1,3-diamine [ No CAS ]

References: [1]Tetrahedron Letters,1996,vol. 37,p. 9207 - 9210.

11
[ 2124-47-2 ]
[ 136539-28-1 ]

References: [1]Journal of Heterocyclic Chemistry,1991,vol. 28,p. 987 - 990.

12
[ 2124-47-2 ]
[ 136539-26-9 ]

References: [1]Journal of Heterocyclic Chemistry,1991,vol. 28,p. 987 - 990.

13
[ 2124-47-2 ]
[ 136572-08-2 ]

References: [1]Journal of Heterocyclic Chemistry,1991,vol. 28,p. 987 - 990.

14
[ 2124-47-2 ]
[ 681463-86-5 ]

References: [1]Gazzetta Chimica Italiana,1903,vol. 33 II,p. 285.
Gazzetta Chimica Italiana,1905,vol. 35 II,p. 370.

15
[ 2124-47-2 ]
4-amino-6-nitro-isophthalic acid dimethyl ester [ No CAS ]

References: [1]Gazzetta Chimica Italiana,1903,vol. 33 II,p. 285.
Gazzetta Chimica Italiana,1905,vol. 35 II,p. 370.

16
[ 2124-47-2 ]
[ 342045-62-9 ]

References: [1]Gazzetta Chimica Italiana,1903,vol. 33 II,p. 285.
Gazzetta Chimica Italiana,1905,vol. 35 II,p. 370.

17
[ 2124-47-2 ]
[ 19871-44-4 ]

References: [1]Journal of the Chemical Society,1906,vol. 89,p. 1294.

18
[ 2124-47-2 ]
4,6,N-trimethyl-m-phenylenediamine [ No CAS ]

References: [1]Journal of the Chemical Society,1907,vol. 91,p. 365.

19
[ 2124-47-2 ]
[ 162100-82-5 ]

References: [1]Recueil des Travaux Chimiques des Pays-Bas,1952,vol. 71,p. 1213,1218.

20
[ 2124-47-2 ]
4-chloro-6-nitro-isophthalic acid [ No CAS ]

References: [1]Recueil des Travaux Chimiques des Pays-Bas,1952,vol. 71,p. 1213,1218.

21
[ 2124-47-2 ]
(2,4-dimethyl-5-nitro-phenyl)-carbamic acid ethyl ester [ No CAS ]

References: [1]Bulletin de la Societe Chimique de France,1899,vol. <3>21,p. 954.

22
[ 2124-47-2 ]
benzenesulfonic acid-(5-amino-2,4,N-trimethyl-anilide) [ No CAS ]

References: [1]Journal of the Chemical Society,1906,vol. 89,p. 1294.

23
[ 2124-47-2 ]
toluene-4-sulfonic acid-(5-amino-2,4,N-trimethyl-anilide) [ No CAS ]

References: [1]Journal of the Chemical Society,1907,vol. 91,p. 365.

24
[ 2124-47-2 ]
4,6,N-trimethyl-2-(4-nitro-phenylazo)-m-phenylenediamine [ No CAS ]

References: [1]Journal of the Chemical Society,1907,vol. 91,p. 365.

25
[ 2124-47-2 ]
toluene-4-sulfonic acid-(2,4,N-trimethyl-5-nitro-anilide) [ No CAS ]

References: [1]Journal of the Chemical Society,1907,vol. 91,p. 365.

26
[ 2124-47-2 ]
1-[2,4-Dimethyl-5-(methyl-nitroso-amino)-phenylazo]-[2]naphthol [ No CAS ]

References: [1]Journal of the Chemical Society,1907,vol. 91,p. 365.

27
[ 2124-47-2 ]
N,N'-bis-(2,4-dimethyl-5-nitro-phenyl)-urea [ No CAS ]

References: [1]Bulletin de la Societe Chimique de France,1899,vol. <3>21,p. 954.

28
[ 2124-47-2 ]
N-methyl-N,N'-(4,6-dimethyl-m-phenylene)-bis-benzenesulfonamide [ No CAS ]

References: [1]Journal of the Chemical Society,1907,vol. 91,p. 365.

29
[ 2124-47-2 ]
benzenesulfonic acid-(5-amino-2,4-dimethyl-anilide) [ No CAS ]

References: [1]Journal of the Chemical Society,1906,vol. 89,p. 1294.

30
[ 2124-47-2 ]
[ 74571-80-5 ]

References: [1]Chemische Berichte,1901,vol. 34,p. 2255.

31
[ 2124-47-2 ]
[ 78831-77-3 ]

References: [1]Chemische Berichte,1901,vol. 34,p. 2255.

32
[ 2124-47-2 ]
5-bromo-2,4-dimethylacetanilide [ No CAS ]

References: [1]Chemische Berichte,1901,vol. 34,p. 2255.

33
[ 2124-47-2 ]
[ 116529-81-8 ]

References: [1]Chemische Berichte,1890,vol. 23,p. 3655.

34
[ 2124-47-2 ]
[ 116632-60-1 ]

References: [1]Chemische Berichte,1890,vol. 23,p. 3655.

35
[ 2124-47-2 ]
N-(6,8-dimethyl-[5]quinolyl)-acetamide [ No CAS ]

References: [1]Chemische Berichte,1890,vol. 23,p. 3655.

36
[ 2124-47-2 ]
[ 4102-50-5 ]

References: [1]Bulletin of the Chemical Society of Japan,1965,vol. 38,p. 1590 - 1595.

37
[ 2124-47-2 ]
[ 4102-52-7 ]

References: [1]Bulletin of the Chemical Society of Japan,1965,vol. 38,p. 1590 - 1595.

38
[ 2124-47-2 ]
[ 69383-69-3 ]

References: [1]Helvetica Chimica Acta,1978,vol. 61,p. 3079 - 3086.

39
[ 2124-47-2 ]
[ 69383-62-6 ]

References: [1]Helvetica Chimica Acta,1978,vol. 61,p. 3079 - 3086.

40
[ 62476-60-2 ]
[ 2124-47-2 ]

Yield	Reaction Conditions	Operation in experiment
	With sulfuric acid; In ethanol; water;	3. Preparation of 2,4-dimethyl-5-nitroaniline A mixture of N-(2,4-dimethyl-5-nitrophenyl)acetamide, water (24 mL), concentrated sulfuric acid (12 mL), and ethanol (120 mL) was heated at reflux under an atmosphere of nitrogen for 4 hours. The ethanol was evaporated under reduced pressure and the residue partitioned between ethyl acetate (250 mL) and brine (150 mL). The brine solution was reextracted with ethyl acetate. The combined ethyl acetate extracts were then dried over magnesium sulfate. Evaporation afforded a crude product which was flash chromatographed on silica and eluted with ethyl acetate:hexane (1:4) to afford 4.63 g as a pale yellow solid.

References: [1]Patent: EP887346,1998,A2 .

41
[ 2124-47-2 ]
[ 62476-60-2 ]

Yield	Reaction Conditions	Operation in experiment
	With acetic anhydride; In dichloromethane;	EXAMPLE 1 Preparation of 2,4-dimethyl-5-nitroacetanilide, using step (1). To a solution of <strong>[2124-47-2]2,4-dimethyl-5-nitroaniline</strong> (16.6 g., 100 mmoles) in methylene chloride (25 ml.), acetic anhydride (14.3 g., 120 mmoles) was added dropwise at 10 to 15 C. The reaction mixture was allowed to come to room temperature and was stirred for 15 minute, whereupon a precipitate started to form. The reaction mixture was heated to reflux for 60 minutes, and was then cooled to 5 to 10 C. The product was collected by filtration, and was washed with hexane. This gave 2,4-dimethyl-5-nitroacetanilide, m.p. 160-164 C.

References: [1]Patent: US4380464,1983,A .

42
[ 16130-58-8 ]
[ 2124-47-2 ]
N-cyanoacetyl-2,4-dimethyl-5-nitroaniline [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
84 g (78%)	With triethylamine; In tetrahydrofuran;	(a) N-Cyanoacetyl-<strong>[2124-47-2]2,4-dimethyl-5-nitroaniline</strong> To a solution of 76.6 g (0.455 mol) of <strong>[2124-47-2]2,4-dimethyl-5-nitroaniline</strong> and 64 ml (0.46 mol) triethylamine in 500 ml abs. tetrahydrofurane is added dropwise within 1 h 47.2 g (0.455 mol) cyanoacetyl chloride in 100 ml tetrahydrofurane. After stirring for 2 h at 25 C. and 3 h at 80 C. and cooling to 25 C. the reaction mixture is filtered and poured into water. The precipitate is separated, washed with water and toluene/petrolether and dried. Yield: 84 g (78%) N-cyanoacetyl-<strong>[2124-47-2]2,4-dimethyl-5-nitroaniline</strong>, mp. 229-230 C.

References: [1]Patent: US4394156,1983,A .

43
5-chloro-3-methoxycarbonyl-2-methyl-4-pyranone [ No CAS ]
[ 2124-47-2 ]
1-(3'-nitro-4',6'-dimethylphenyl)-5-chloro-3-methoxycarbonyl-2-methyl-4-pyridone [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
15.0 g (85.5%)	With p-toluenesulfonic acid monohydrate; In water; toluene;	(a) 1-(3'-Nitro-4',6'-dimethylphenyl)-5-chloro-3-methoxycarbonyl-2-methyl-4-pyridone A solution of 10.1 g (0.05 mol) 5-chloro-3-methoxycarbonyl-2-methyl-4-pyranone, 8.5 g <strong>[2124-47-2]2,4-dimethyl-5-nitroaniline</strong> and 0.1 g p-toluenesulfonic acid monohydrate in 100 ml of toluene are refluxed for 8 h in a water separator apparatus. The mixture is allowed to cool and the precipitating product is filtered off, washed with a small amount of ethylacetate/petrolether and dried. Yield: 15.0 g (85.5%) 1-(3'-nitro-4',6'-dimethylphenyl)-5-chloro-3-methoxycarbonyl-2-methyl-4-pyridone, mp. 266 C.

References: [1]Patent: US4394156,1983,A .

44
mononitro-2,4-dimethylaniline [ No CAS ]
[ 1635-84-3 ]
[ 31167-04-1 ]
[ 2124-47-2 ]
[ 95-68-1 ]
mononitro-2,4-dimethylacetanilide [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	With acetic anhydride; In water; acetic acid;	EXAMPLE 3a Preparation of the mononitro-2,4-dimethylacetanilide isomer mixture 300 g (5.0 mols) of glacial acetic acid are initially introduced into a 1 l four-necked flask with a stirrer, condenser, dropping funnel and internal thermometer. 141 g of mononitro-2,4-dimethylaniline isomer mixture (prepared by nitration of 121 g=1.0 mol of 2,4-dimethylaniline) of the following composition: 90.2% by weight of <strong>[2124-47-2]5-nitro-2,4-dimethylaniline</strong>, 9.5% by weight of 3-nitro-2,4-dimethylaniline, and 0.3% by weight of 6-nitro-2,4-dimethylaniline are introduced into the flask at 20 C. 122 g (1.2 mols) of acetic anhydride are added dropwise to the mixture in the course of 1 hour, whilst cooling, and the temperature is not to rise above 55 C. The reaction mixture is then heated to boiling and is heated under reflux for 1 hour. 300 g is glacial acetic acid are then distilled off under normal pressure. The approximately 120 C. hot reaction solution is allowed to run into an initially introduced quantity of 1,500 g of water at 35 C., whilst stirring, and the temperature is not to rise above 60 C. The reaction mixture is cooled to 20 C., whilst stirring, and the precipitated product is filtered, washed with water until free from acetic acid and dried well under suction. Yield about 230 g of moist product with the relative composition given above.

References: [1]Patent: US4540817,1985,A .

45
[ 2124-47-2 ]
copper(l) chloride [ No CAS ]
[ 69383-68-2 ]

Yield	Reaction Conditions	Operation in experiment
47%	With sodium nitrite; In hydrogenchloride; water;	4-Chloro-6-nitro-m-xylene A solution of sodium nitrite (7.2 g, 0.1 mol) in water (20 mL) was added dropwise over 45 min at <5 C to a stirred suspension of 5-nitro-2,4-xylidine (16.6 g, 0.1 mol) in conc. hydrochloric acid (300 mL). After complete addition the reaction was stirred at <5 C for 1 h then a solution of copper(I)chloride (16.0 g, 0.16 mol) in conc. hydrochloric acid (50 mL) was added dropwise over 20 min at <5 C (CARE: effervescence at first). The reaction was then warmed from 0 C to room temperature and stirred for 18 h. The mixture was then carefully poured into water (1 L) and extracted with ethyl acetate (3 x 300 mL). The combined organic extracts were dried (magnesium sulfate), filtered and the solvent removed under vacuum to leave a crude oil. The oil was purified by flash column chromatography (SiO2; heptane) to give the product as a yellow oil (8.8 g, 47%). IR numax (film)/cm-1 3103, 2985, 2935, 2863, 2744, 2432, 1610, 1572, 1518, 1480, 1454, 1384, 1346, 1286, 1266, 1244, 1197, 1166, 1157, 1107, 1036, 982, 894, 842, 759, 746, 725, 704, 646 and 602; NMR deltaH (400 MHz; CDCl3) 8.01 (1H, s), 7.20 (1H, s), 2.56 (3H, s), 2.41 (3H, s).

References: [1]Patent: EP1147110,2003,B1 .

46
[ 2124-47-2 ]
[ 72521-00-7 ]

Yield	Reaction Conditions	Operation in experiment
58.1%	With acetic acid; sodium nitrite; In water; at 0 - 25℃;	Preparation 6; 1-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-5-methyl-1H-indazol-6-ylamineThe synthetic procedure used in this preparation is outlined in Scheme F. Step 1 5-Methyl-6-nitro-1H-indazole<strong>[2124-47-2]2,4-Dimethyl-5-nitroaniline</strong> (1.662 g, 10.00 mmol) was dissolved in glacial acetic acid (100 ml) and the mixture was cooled to 0 C. A solution of sodium nitrite (1 eq, 690 mg) in water (2 ml) was added while maintaining a temperature below 25 C. Stirring was continued for three hours and the mixture was filtered. The filtrate was allowed to stand for three days at room temperature, then was concentrate under reduced pressure. The residue was diluted with water and the resulting mixture was stirred vigorously. The solid product was collected by filtration, washed thoroughly with cold water, and dried. The product was purified by flash chromatography (99:1 dichloromethane/methanol) to give 1.030 g (58.1%) of 5-methyl-6-nitro-1H-indazole as a solid.
58.1%	With acetic acid; sodium nitrite; In water; at 0 - 25℃;	Step 1 5-Methyl-6-nitro-1H-indazole<strong>[2124-47-2]2,4-Dimethyl-5-nitroaniline</strong> (1.662 g, 10.00 mmol) was dissolved in glacial acetic acid (100 ml) and the mixture was cooled to 0 C. A solution of sodium nitrite (1 eq, 690 mg) in water (2 ml) was added while maintaining a temperature below 25 C. Stirring was continued for three hours and the mixture was filtered. The filtrate was allowed to stand for three days at room temperature, then was concentrate under reduced pressure. The residue was diluted with water and the resulting mixture was stirred vigorously. The solid product was collected by filtration, washed thoroughly with cold water, and dried. The product was purified by flash chromatography (99:1 dichloromethane/methanol) to give 1.030 g (58.1%) of 5-methyl-6-nitro-1H-indazole as a solid.
		Example 168; Synthesis of 6-piperazin-l-yl-2-(2-trifluoromethyl-phenylamino)-lH-benzoimidazole-5- carboxylic acid (5-methyl-lH-indazol-6-yl)amideTo a mixture of 2,4-dimethylaniline (10 mmol) in 5 mL of cone. H2SO4, fuming HNO3 (90%; 0.6 mL) was added dropwise at 0 0C. The resulting mixture was stirred for 12 h at RT and then slowly poured into ice. The solid was collected by filtration and dried to yield <strong>[2124-47-2]2,4-dimethyl-5-nitroaniline</strong> as a yellow solid.A solution of nitroaniline (5 mmol) obtained as above in HOAc (5 mL) at RT was added with zso-amyl nitrite (6 mmol) dropwise. The resulting mixture was stirred at RT for 14 h and then slowly poured on to cold saturated aqueous NaHCO3 solution (15 mL). The contents were extracted with ethyl acetate (3 x 20 mL), and the combined organics was washed with 5% aqueous Na2Ctheta3 solution (30 mL). The volatiles were removed in vacuo to give 6-nitro-5-methylindazole as a brown solid.The nitro compound (2 mmol) obtained as above was reduced under hydrogenation conditions as described in general procedure F to afford 6-amino-5-methylindazole as a brown solid. The aminoindazole from above (1.5 mmol) was reacted with 4-chloro-2-fluoro-5- nitrobenzoyl chloride (1.5 mmol) employing the conditions described in Example 115. The product, 2-chloro-4-fluoro-N-(5-methyl-lH-indazol-6-yl)-5-nitrobenzamide, was also isolated similar to Example 115.A solution of the amide from above (1 mmol) in dioxane (2 mL) was reacted with aqueous NH4OH using the conditions described in Example 115. After the formation of 4- <n="92"/>amino-2-chloro-N-(5-methyl-lH-indazol-6-yl)-5-nitrobenzamide was complete, charged with piperazine (5 mmol). The contents were heated at reflux for 1O h and the reaction mixture was cooled to RT. The contents were poured onto ice cold water with vigorous stirring. The solid formed was collected by filtration, washed with water, and dried in vacuo to provide the product, 4-amino-N-(5-methyl-lH-indazol-6-yl)-5-nitro-2-piperazin-l-yl-benzamide as a yellow solid.The product from above (0.6 mol) was treated with BOC anhydride employing the procedure described for Example 163.The nitro aniline from above (0.5 mmol) was reduced under hydrogenation conditions as described in general procedure F to afford 4-[4,5-diamino-2-(5-methyl-lH-mdazol-6- ylcarbamoyl)-phenyl]piperazine-l-carboxylic acid tert-butyl ester.The diamine (0.3 mmol) from above was reacted with l-isothiocyanato-2- trifluoromethylbenzene (0.3 mmol) followed by cyclization in situ using EDC as described in general procedure B to provide 4-[6-(5-Methyl-lH-indazol-6-ylcarbamoyl)-2-(2- trifluoromethyl-phenylamino)-3H-benzoimidazol-5-yl]piperazine-l-carboxylic acid tert-butyl ester. MS: m/z 635 (M+H)+.The product from above was treated with 4M HCl in dioxane employing the procedure described for Example 156 to afford 6-piperazin-l-yl-2-(2-trifluoromethyl- phenylamino)-lH-benzoimidazole-5-carboxylic acid (5-methyl-lH-indazol-6-yl)amide as a hydrochloride salt. MS: m/z 535 (M+H)+.

References: [1]Bioorganic and Medicinal Chemistry,2016,vol. 24,p. 403 - 427.
[2]Patent: US2010/160373,2010,A1 .Location in patent: Page/Page column 28-29.
[3]Patent: US2011/71143,2011,A1 .Location in patent: Page/Page column 37.
[4]Journal of Medicinal Chemistry,2015,vol. 58,p. 8413 - 8426.
[5]Patent: WO2007/95124,2007,A2 .Location in patent: Page/Page column 89-90.

47
[ 335-05-7 ]
[ 2124-47-2 ]
[ 75-50-3 ]
[ 53780-35-1 ]

References: [1]Gmelin Handbuch der Anorganischen Chemie,Gmelin Handbook: F: PerFHalOrg.SVol.3, 6.2.3.4, page 152 - 186.
[2]Patent: US4013444,1977,A .

48
[ 110-99-6 ]
[ 2124-47-2 ]
2,4,8,10-tetramethyl-1,7-dinitro-6H,12H-5,11-methanodibenzo[b,f][1,5]diazocine [ No CAS ]

References: [1]European Journal of Organic Chemistry,2009,p. 687 - 698.

49
[ 2124-47-2 ]
[ 1232685-13-0 ]

References: [1]Patent: US2011/71143,2011,A1 .
[2]Journal of Medicinal Chemistry,2015,vol. 58,p. 8413 - 8426.

50
[ 2124-47-2 ]
[ 1232685-12-9 ]

References: [1]Patent: US2011/71143,2011,A1 .
[2]Journal of Medicinal Chemistry,2015,vol. 58,p. 8413 - 8426.

51
[ 2124-47-2 ]
[ 1273550-56-3 ]

References: [1]Patent: US2011/71143,2011,A1 .

52
[ 2124-47-2 ]
[ 1273549-97-5 ]

References: [1]Patent: US2011/71143,2011,A1 .

53
[ 2124-47-2 ]
[ 1273550-55-2 ]

References: [1]Patent: US2011/71143,2011,A1 .

54
[ 2124-47-2 ]
[ 1273550-45-0 ]

References: [1]Patent: US2011/71143,2011,A1 .

Historical Records

Technical Information

• Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chan-Lam Coupling Reaction • Hydride Reductions • Leuckart-Wallach Reaction • Mannich Reaction • Petasis Reaction • Preparation of Amines • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Specialized Acylation Reagents-Vilsmeier Reagent • Ugi Reaction

Related Functional Groups of
[ 2124-47-2 ]

Aryls

A120506 [6629-29-4]

4-Methyl-5-nitrobenzene-1,3-diamine

Similarity: 1.00

A210503 [35572-78-2]

2-Methyl-3,5-dinitroaniline

Similarity: 1.00

A140527 [106837-44-9]

2,3-Dimethyl-5-nitroaniline

Similarity: 0.95

A614229 [611-05-2]

3-Methyl-4-nitroaniline

Similarity: 0.93

A136993 [20191-74-6]

2-Ethyl-5-nitroaniline

Similarity: 0.91

Amines

A120506 [6629-29-4]

4-Methyl-5-nitrobenzene-1,3-diamine

Similarity: 1.00

A210503 [35572-78-2]

2-Methyl-3,5-dinitroaniline

Similarity: 1.00

A140527 [106837-44-9]

2,3-Dimethyl-5-nitroaniline

Similarity: 0.95

A614229 [611-05-2]

3-Methyl-4-nitroaniline

Similarity: 0.93

A136993 [20191-74-6]

2-Ethyl-5-nitroaniline

Similarity: 0.91

Nitroes

A120506 [6629-29-4]

4-Methyl-5-nitrobenzene-1,3-diamine

Similarity: 1.00

A210503 [35572-78-2]

2-Methyl-3,5-dinitroaniline

Similarity: 1.00

A140527 [106837-44-9]

2,3-Dimethyl-5-nitroaniline

Similarity: 0.95

A614229 [611-05-2]

3-Methyl-4-nitroaniline

Similarity: 0.93

A136993 [20191-74-6]

2-Ethyl-5-nitroaniline

Similarity: 0.91

Precautionary Statements-General
Code	Phrase
P101	If medical advice is needed,have product container or label at hand.
P102	Keep out of reach of children.
P103	Read label before use
Prevention
Code	Phrase
P201	Obtain special instructions before use.
P202	Do not handle until all safety precautions have been read and understood.
P210	Keep away from heat/sparks/open flames/hot surfaces. - No smoking.
P211	Do not spray on an open flame or other ignition source.
P220	Keep/Store away from clothing/combustible materials.
P221	Take any precaution to avoid mixing with combustibles
P222	Do not allow contact with air.
P223	Keep away from any possible contact with water, because of violent reaction and possible flash fire.
P230	Keep wetted
P231	Handle under inert gas.
P232	Protect from moisture.
P233	Keep container tightly closed.
P234	Keep only in original container.
P235	Keep cool
P240	Ground/bond container and receiving equipment.
P241	Use explosion-proof electrical/ventilating/lighting/equipment.
P242	Use only non-sparking tools.
P243	Take precautionary measures against static discharge.
P244	Keep reduction valves free from grease and oil.
P250	Do not subject to grinding/shock/friction.
P251	Pressurized container: Do not pierce or burn, even after use.
P260	Do not breathe dust/fume/gas/mist/vapours/spray.
P261	Avoid breathing dust/fume/gas/mist/vapours/spray.
P262	Do not get in eyes, on skin, or on clothing.
P263	Avoid contact during pregnancy/while nursing.
P264	Wash hands thoroughly after handling.
P265	Wash skin thouroughly after handling.
P270	Do not eat, drink or smoke when using this product.
P271	Use only outdoors or in a well-ventilated area.
P272	Contaminated work clothing should not be allowed out of the workplace.
P273	Avoid release to the environment.
P280	Wear protective gloves/protective clothing/eye protection/face protection.
P281	Use personal protective equipment as required.
P282	Wear cold insulating gloves/face shield/eye protection.
P283	Wear fire/flame resistant/retardant clothing.
P284	Wear respiratory protection.
P285	In case of inadequate ventilation wear respiratory protection.
P231 + P232	Handle under inert gas. Protect from moisture.
P235 + P410	Keep cool. Protect from sunlight.
Response
Code	Phrase
P301	IF SWALLOWED:
P304	IF INHALED:
P305	IF IN EYES:
P306	IF ON CLOTHING:
P307	IF exposed:
P308	IF exposed or concerned:
P309	IF exposed or if you feel unwell:
P310	Immediately call a POISON CENTER or doctor/physician.
P311	Call a POISON CENTER or doctor/physician.
P312	Call a POISON CENTER or doctor/physician if you feel unwell.
P313	Get medical advice/attention.
P314	Get medical advice/attention if you feel unwell.
P315	Get immediate medical advice/attention.
P320
P302 + P352	IF ON SKIN: wash with plenty of soap and water.
P321
P322
P330	Rinse mouth.
P331	Do NOT induce vomiting.
P332	IF SKIN irritation occurs:
P333	If skin irritation or rash occurs:
P334	Immerse in cool water/wrap n wet bandages.
P335	Brush off loose particles from skin.
P336	Thaw frosted parts with lukewarm water. Do not rub affected area.
P337	If eye irritation persists:
P338	Remove contact lenses, if present and easy to do. Continue rinsing.
P340	Remove victim to fresh air and keep at rest in a position comfortable for breathing.
P341	If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P342	If experiencing respiratory symptoms:
P350	Gently wash with plenty of soap and water.
P351	Rinse cautiously with water for several minutes.
P352	Wash with plenty of soap and water.
P353	Rinse skin with water/shower.
P360	Rinse immediately contaminated clothing and skin with plenty of water before removing clothes.
P361	Remove/Take off immediately all contaminated clothing.
P362	Take off contaminated clothing and wash before reuse.
P363	Wash contaminated clothing before reuse.
P370	In case of fire:
P371	In case of major fire and large quantities:
P372	Explosion risk in case of fire.
P373	DO NOT fight fire when fire reaches explosives.
P374	Fight fire with normal precautions from a reasonable distance.
P376	Stop leak if safe to do so. Oxidising gases (section 2.4) 1
P377	Leaking gas fire: Do not extinguish, unless leak can be stopped safely.
P378
P380	Evacuate area.
P381	Eliminate all ignition sources if safe to do so.
P390	Absorb spillage to prevent material damage.
P391	Collect spillage. Hazardous to the aquatic environment
P301 + P310	IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P301 + P312	IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P301 + P330 + P331	IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P302 + P334	IF ON SKIN: Immerse in cool water/wrap in wet bandages.
P302 + P350	IF ON SKIN: Gently wash with plenty of soap and water.
P303 + P361 + P353	IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P304 + P312	IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell.
P304 + P340	IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P304 + P341	IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P305 + P351 + P338	IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P306 + P360	IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes.
P307 + P311	IF exposed: call a POISON CENTER or doctor/physician.
P308 + P313	IF exposed or concerned: Get medical advice/attention.
P309 + P311	IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician.
P332 + P313	IF SKIN irritation occurs: Get medical advice/attention.
P333 + P313	IF SKIN irritation or rash occurs: Get medical advice/attention.
P335 + P334	Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages.
P337 + P313	IF eye irritation persists: Get medical advice/attention.
P342 + P311	IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician.
P370 + P376	In case of fire: Stop leak if safe to Do so.
P370 + P378	In case of fire:
P370 + P380	In case of fire: Evacuate area.
P370 + P380 + P375	In case of fire: Evacuate area. Fight fire remotely due to the risk of explosion.
P371 + P380 + P375	In case of major fire and large quantities: Evacuate area. Fight fire remotely due to the risk of explosion.
Storage
Code	Phrase
P401
P402	Store in a dry place.
P403	Store in a well-ventilated place.
P404	Store in a closed container.
P405	Store locked up.
P406	Store in corrosive resistant/ container with a resistant inner liner.
P407	Maintain air gap between stacks/pallets.
P410	Protect from sunlight.
P411
P412	Do not expose to temperatures exceeding 50 oC/ 122 oF.
P413
P420	Store away from other materials.
P422
P402 + P404	Store in a dry place. Store in a closed container.
P403 + P233	Store in a well-ventilated place. Keep container tightly closed.
P403 + P235	Store in a well-ventilated place. Keep cool.
P410 + P403	Protect from sunlight. Store in a well-ventilated place.
P410 + P412	Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF.
P411 + P235	Keep cool.
Disposal
Code	Phrase
P501	Dispose of contents/container to ...
P502	Refer to manufacturer/supplier for information on recovery/recycling

Physical hazards
Code	Phrase
H200	Unstable explosive
H201	Explosive; mass explosion hazard
H202	Explosive; severe projection hazard
H203	Explosive; fire, blast or projection hazard
H204	Fire or projection hazard
H205	May mass explode in fire
H220	Extremely flammable gas
H221	Flammable gas
H222	Extremely flammable aerosol
H223	Flammable aerosol
H224	Extremely flammable liquid and vapour
H225	Highly flammable liquid and vapour
H226	Flammable liquid and vapour
H227	Combustible liquid
H228	Flammable solid
H229	Pressurized container: may burst if heated
H230	May react explosively even in the absence of air
H231	May react explosively even in the absence of air at elevated pressure and/or temperature
H240	Heating may cause an explosion
H241	Heating may cause a fire or explosion
H242	Heating may cause a fire
H250	Catches fire spontaneously if exposed to air
H251	Self-heating; may catch fire
H252	Self-heating in large quantities; may catch fire
H260	In contact with water releases flammable gases which may ignite spontaneously
H261	In contact with water releases flammable gas
H270	May cause or intensify fire; oxidizer
H271	May cause fire or explosion; strong oxidizer
H272	May intensify fire; oxidizer
H280	Contains gas under pressure; may explode if heated
H281	Contains refrigerated gas; may cause cryogenic burns or injury
H290	May be corrosive to metals
Health hazards
Code	Phrase
H300	Fatal if swallowed
H301	Toxic if swallowed
H302	Harmful if swallowed
H303	May be harmful if swallowed
H304	May be fatal if swallowed and enters airways
H305	May be harmful if swallowed and enters airways
H310	Fatal in contact with skin
H311	Toxic in contact with skin
H312	Harmful in contact with skin
H313	May be harmful in contact with skin
H314	Causes severe skin burns and eye damage
H315	Causes skin irritation
H316	Causes mild skin irritation
H317	May cause an allergic skin reaction
H318	Causes serious eye damage
H319	Causes serious eye irritation
H320	Causes eye irritation
H330	Fatal if inhaled
H331	Toxic if inhaled
H332	Harmful if inhaled
H333	May be harmful if inhaled
H334	May cause allergy or asthma symptoms or breathing difficulties if inhaled
H335	May cause respiratory irritation
H336	May cause drowsiness or dizziness
H340	May cause genetic defects
H341	Suspected of causing genetic defects
H350	May cause cancer
H351	Suspected of causing cancer
H360	May damage fertility or the unborn child
H361	Suspected of damaging fertility or the unborn child
H361d	Suspected of damaging the unborn child
H362	May cause harm to breast-fed children
H370	Causes damage to organs
H371	May cause damage to organs
H372	Causes damage to organs through prolonged or repeated exposure
H373	May cause damage to organs through prolonged or repeated exposure
Environmental hazards
Code	Phrase
H400	Very toxic to aquatic life
H401	Toxic to aquatic life
H402	Harmful to aquatic life
H410	Very toxic to aquatic life with long-lasting effects
H411	Toxic to aquatic life with long-lasting effects
H412	Harmful to aquatic life with long-lasting effects
H413	May cause long-lasting harmful effects to aquatic life
H420	Harms public health and the environment by destroying ozone in the upper atmosphere

{[proInfo.proName]}

CAS No.: 2124-47-2

{[proInfo.proName]}

CAS No.: 2124-47-2

Alternative Products

Product Details of [ 2124-47-2 ]

Safety of [ 2124-47-2 ]

Computational Chemistry of [ 2124-47-2 ] Show Less

Physicochemical Properties

Lipophilicity

Water Solubility

Pharmacokinetics

Druglikeness

Medicinal Chemistry

Application In Synthesis of [ 2124-47-2 ]

[ 2124-47-2 ] Synthesis Path-Upstream 1~2

[ 2124-47-2 ] Synthesis Path-Downstream 1~54

Related Products

Historical Records

Technical Information

Categories

Related Functional Groups of
[ 2124-47-2 ]

Aryls

Amines

Nitroes

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

Inquiry

Molarity Calculator

Total Compounds Calculator

Dissolution Calculator

{[proInfo.proName]}

CAS No.: 2124-47-2

{[proInfo.proName]}

CAS No.: 2124-47-2

Alternative Products

Product Details of [ 2124-47-2 ]

Safety of [ 2124-47-2 ]

Computational Chemistry of [ 2124-47-2 ] Show Less

Physicochemical Properties

Lipophilicity

Water Solubility

Pharmacokinetics

Druglikeness

Medicinal Chemistry

Application In Synthesis of [ 2124-47-2 ]

[ 2124-47-2 ] Synthesis Path-Upstream 1~2

[ 2124-47-2 ] Synthesis Path-Downstream 1~54

Related Products

Historical Records

Technical Information

Categories

Related Functional Groups of [ 2124-47-2 ]

Aryls

Amines

Nitroes

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

Inquiry

Molarity Calculator

Total Compounds Calculator

Dissolution Calculator

Related Functional Groups of
[ 2124-47-2 ]