Clonazepam Related Compound B | Chlorides

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Quality Control of Clonazepam Related Compound B Purity: 97% SDS Specification

COA

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NMR

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Product Details of Clonazepam Related Compound B

CAS No. :	2011-66-7
Formula :	C₁₃H₉ClN₂O₃
M.W :	276.68
SMILES Code :	O=C(C1=CC([N+]([O-])=O)=CC=C1N)C2=CC=CC=C2Cl
MDL No. :	MFCD00792453
InChI Key :	GRDGBWVSVMLKBV-UHFFFAOYSA-N
Pubchem ID :	74830

Safety of Clonazepam Related Compound B

GHS Pictogram:
Signal Word:	Warning
Hazard Statements:	H341
Precautionary Statements:	P201-P308+P313

Application In Synthesis of Clonazepam Related Compound B

* 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.

Downstream synthetic route of [ 2011-66-7 ]

[ 2011-66-7 ] Synthesis Path-Downstream 1~29

1
[ 97-97-2 ]
[ 2011-66-7 ]
[ 101945-55-5 ]

References: [1]European Journal of Medicinal Chemistry,1985,vol. 20,p. 541 - 546.

2
[ 15050-24-5 ]
[ 2011-66-7 ]
[ 76337-80-9 ]

References: [1]Journal of Medicinal Chemistry,1981,vol. 24,p. 20 - 27.

3
[ 2011-66-7 ]
[ 1937-19-5 ]
[ 136623-22-8 ]

References: [1]Pharmazie,1992,vol. 47,p. 758 - 764.

4
[ 2011-66-7 ]
[ 54534-72-4 ]

Yield	Reaction Conditions	Operation in experiment
	With hydrogenchloride;copper(I) chloride; In water; acetic acid; sodium nitrite;	EXAMPLE 26 (2-Chloro-5-nitrophenyl)(2-chlorophenyl)methanone To 180 ml of concentrated sulfuric acid cooled to 0 in an ice bath was added 28 g (0.4 mol) of sodium nitrite in portions at such a rate that the temperature did not go above 10. This mixture was warmed on a steam bath until a solution formed. It was then cooled to 30 and a solution of 110.68 g (0.4 mol) of <strong>[2011-66-7]2-amino-5-nitro-2'-chlorobenzophenone</strong> in 300 mL of hot acetic acid was added at such a rate that the temperature did not exceed 40. This mixture was stirred without heating for 2.5 hr, and then poured slowly into a mixture of 800 mL of concentrated hydrochloric acid and 80 g of cuprous chloride. This mixture was heated to 80 on a steam bath for 40 min until the foaming had subsided, poured into 2 l of water, and allowed to stand overnight. The solid was collected, washed with water and recrystallized from methanol to give product, mp 76-79. An analytical sample prepared by recrystallization from methanol had mp 78.5-80.

References: [1]Journal of Medicinal Chemistry,1991,vol. 34,p. 1545 - 1552.
[2]Patent: US4379765,1983,A .

5
[ 55501-45-6 ]
[ 609-65-4 ]
[ 2011-66-7 ]

References: [1]Journal of Medicinal Chemistry,1991,vol. 34,p. 1545 - 1552.

6
[ 2011-66-7 ]
[ 56218-62-3 ]
[ 80837-64-5 ]

References: [1]Pharmazie,1981,vol. 36,p. 668 - 671.

7
[ 61197-73-7 ]
[ 2011-66-7 ]

References: [1]Archiv der Pharmazie,1991,vol. 324,p. 417 - 421.

8
[ 364046-84-4 ]
[ 2011-66-7 ]

References: [1]Journal of Medicinal Chemistry,1963,vol. 6,p. 261 - 265.

10
[ 2011-66-7 ]
[ 108-94-1 ]
7-nitro-9-(2-nitro-phenyl)-1,2,3,4-tetrahydro-acridine [ No CAS ]

References: [1]Tetrahedron Letters,2005,vol. 46,p. 7249 - 7253.

11
[ 2011-66-7 ]
[ 141-97-9 ]
2-methyl-6-nitro-4-(2-nitro-phenyl)-quinoline-3-carboxylic acid ethyl ester [ No CAS ]

References: [1]Tetrahedron Letters,2005,vol. 46,p. 7249 - 7253.

12
[ 2011-66-7 ]
[ 123-54-6 ]
1-[2-methyl-6-nitro-4-(2-nitro-phenyl)-quinolin-3-yl]-ethanone [ No CAS ]

References: [1]Tetrahedron Letters,2005,vol. 46,p. 7249 - 7253.

13
[ 2011-66-7 ]
[ 101928-09-0 ]

References: [1]European Journal of Medicinal Chemistry,1985,vol. 20,p. 541 - 546.

14
[ 2011-66-7 ]
[ 101928-10-3 ]

References: [1]European Journal of Medicinal Chemistry,1985,vol. 20,p. 541 - 546.

15
[ 2011-66-7 ]
[ 101928-12-5 ]

References: [1]European Journal of Medicinal Chemistry,1985,vol. 20,p. 541 - 546.

16
[ 2011-66-7 ]
[ 101928-11-4 ]

References: [1]European Journal of Medicinal Chemistry,1985,vol. 20,p. 541 - 546.

17
[ 2011-66-7 ]
[ 101928-13-6 ]

References: [1]European Journal of Medicinal Chemistry,1985,vol. 20,p. 541 - 546.

18
[ 2011-66-7 ]
[ 101928-18-1 ]

References: [1]European Journal of Medicinal Chemistry,1985,vol. 20,p. 541 - 546.

19
[ 2011-66-7 ]
[ 88968-21-2 ]

References: [1]European Journal of Medicinal Chemistry,1985,vol. 20,p. 541 - 546.

20
[ 2011-66-7 ]
[ 86187-94-2 ]

References: [1]Journal of Medicinal Chemistry,1991,vol. 34,p. 1545 - 1552.

21
[ 2011-66-7 ]
[ 113456-71-6 ]

References: [1]Journal of Medicinal Chemistry,1991,vol. 34,p. 1545 - 1552.

22
[ 1142-20-7 ]
[ 2011-66-7 ]
[ 58662-82-1 ]

Yield	Reaction Conditions	Operation in experiment
	With thionyl chloride; sodium hydrogencarbonate; In tetrahydrofuran; Petroleum ether;	(a) 53.6 g of carbobenzoxy-L-alanine are dissolved in 400 ml of dry tetrahydrofuran, the solution is treated dropwise with 30 g of thionyl chloride while cooling with ice and the mixture is stirred for 1 hour in the cold. A solution of 54 g (0.2 mol) of <strong>[2011-66-7]2-amino-5-nitro-2'-chlorobenzophenone</strong> in 150 ml of dry tetrahydrofuran is subsequently added dropwise thereto rapidly, whereupon the mixture is stirred at room temperature for 24 hours. The solution obtained is concentrated, the residue is treated with ice and 10 percent sodium bicarbonate solution and extracted with methylene chloride. The organic solution is dried over sodium sulphate and evaporated. The residue is treated with dry ether, left to crystallize for 1 hour and then filtered while rinsing with ether/petroleum ether (1:1). After drying, there is obtained (S)-benzyl-[1-[[2-(o-chlorobenzoyl)-4-nitrophenyl]carbamoyl]ethyl]carbamate of melting point 143-145; [alpha]25 D =18 (1 percent solution in methylene chloride).

References: [1]Patent: US4474777,1984,A .

23
[ 2011-66-7 ]
[ 7772-99-8 ]
[ 58479-51-9 ]

Yield	Reaction Conditions	Operation in experiment
	With sodium hydroxide; In hydrogenchloride;	(a) 100 g of <strong>[2011-66-7]2-amino-2'-chloro-5-nitrobenzophenone</strong> are suspended in 865 ml of 25% hydrochloric acid and treated portionwise with a total of 269 g of tin (II) chloride. The mixture is stirred at room temperature for 36 hours, then diluted with 0.5 l of an ice/water mixture and adjusted to pH 10 with about 2.17 l of a 28% sodium hydroxide solution. The mixture is extracted with methylene chloride. After evaporation of the solvent, the residue is dissolved in 0.54 l of ether and crystallized at about -20. There is obtained 2,5-diamino-2'-chlorobenzophenone of melting point 30-40.

References: [1]Patent: US4464300,1984,A .

24
[ 2011-66-7 ]
2-amino-2'-chloro-5-nitrobenzophenone hydrazone [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	With hydrazine hydrate; In diethylene glycol;	Preparation 4 2-Amino-2'-chloro-5-nitrobenzophenone hydrazone In the manner given in Preparation 1, <strong>[2011-66-7]2-amino-2'-chloro-5-nitrobenzophenone</strong> is refluxed with hydrazine hydrate in diethylene glycol to give <strong>[2011-66-7]2-amino-2'-chloro-5-nitrobenzophenone</strong> hydrazone.

References: [1]Patent: US3941802,1976,A .

25
[ 1142-20-7 ]
[ 2011-66-7 ]
[ 80080-94-0 ]

Yield	Reaction Conditions	Operation in experiment
	With phosphorus pentachloride; In tetrahydrofuran; toluene;	82 g of carbobenzoxy-L-alanine are dissolved in 100 ml of absolute tetrahydrofuran, the solution is cooled to -40 C and treated with 80 g of phosphorus pentachloride. The mixture is stirred at -30 C for 20 minutes and subsequently added to a shaken solution of 80 g of <strong>[2011-66-7]2-amino-5-nitro-2'-chlorobenzophenone</strong> in 100 ml of absolute tetrahydrofuran. The solution is concentrated on a rotary evaporator at 50-60 C, treated twice with toluene and evaporated each time. By crystallisation of the residue from ether, there is obtained (-)-benzyl-[1-[{2-(o-chlorobenzoyl)4-nitrophenyl}carbamoyl]-ethyl]carbamate which melts at 147 C and exhibits a rotation of [alpha]25D =-18.2 (in methylene chloride, 1%).

References: [1]Patent: US4031078,1977,A .

26
[ 609-65-4 ]
[ 100-01-6 ]
[ 2011-66-7 ]

References: [1]Medicinal Chemistry Research,2013,vol. 22,p. 5901 - 5911.

27
[ 2011-66-7 ]
2-{N,N-bis(2'-chloroethyl)}aminoacetamido-2'-chloro-5-nitrobenzophenone [ No CAS ]

References: [1]Medicinal Chemistry Research,2013,vol. 22,p. 5901 - 5911.
[2]Medicinal Chemistry Research,2013,vol. 22,p. 5901 - 5911.

28
[ 2011-66-7 ]
[ 598-21-0 ]
2-bromo-2'-(2-chlorobenzoyl)-4'-nitroacetanilide [ No CAS ]

References: [1]Medicinal Chemistry Research,2013,vol. 22,p. 5901 - 5911.

29
[ 2011-66-7 ]
[ 1779-49-3 ]
2-(1-(2-chlorophenyl)vinyl)-4-nitroaniline [ No CAS ]

References: [1]Organic and Biomolecular Chemistry,2017,vol. 15,p. 6318 - 6322.

Historical Records

Technical Information

• Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chan-Lam Coupling Reaction • Clemmensen Reduction • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Lawesson's Reagent • Leuckart-Wallach Reaction • Mannich Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reformatsky Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Specialized Acylation Reagents-Vilsmeier Reagent • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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Code	Phrase
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P312	Call a POISON CENTER or doctor/physician if you feel unwell.
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P314	Get medical advice/attention if you feel unwell.
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P321
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P342	If experiencing respiratory symptoms:
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P351	Rinse cautiously with water for several minutes.
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P353	Rinse skin with water/shower.
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P376	Stop leak if safe to do so. Oxidising gases (section 2.4) 1
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P378
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P390	Absorb spillage to prevent material damage.
P391	Collect spillage. Hazardous to the aquatic environment
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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.
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P370 + P376	In case of fire: Stop leak if safe to Do so.
P370 + P378	In case of fire:
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P371 + P380 + P375	In case of major fire and large quantities: Evacuate area. Fight fire remotely due to the risk of explosion.
Storage
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P401
P402	Store in a dry place.
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P411
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P413
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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.
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Disposal
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P501	Dispose of contents/container to ...
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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
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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
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Health hazards
Code	Phrase
H300	Fatal if swallowed
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H302	Harmful if swallowed
H303	May be harmful if swallowed
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H310	Fatal in contact with skin
H311	Toxic in contact with skin
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H314	Causes severe skin burns and eye damage
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H316	Causes mild skin irritation
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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

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CAS No.: 2011-66-7

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CAS No.: 2011-66-7

Alternative Products

Product Details of Clonazepam Related Compound B

Safety of Clonazepam Related Compound B

Application In Synthesis of Clonazepam Related Compound B

[ 2011-66-7 ] Synthesis Path-Downstream 1~29

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Technical Information

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Precautionary Statements-General

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