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[ CAS No. 6142-05-8 ]

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Chemical Structure| 6142-05-8
Chemical Structure| 6142-05-8
Structure of 6142-05-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 6142-05-8 ]

CAS No. :6142-05-8 MDL No. :MFCD00270826
Formula : C3H5ClN2S Boiling Point : -
Linear Structure Formula :- InChI Key :WDJXDOCQCALXMV-UHFFFAOYSA-N
M.W :136.60 g/mol Pubchem ID :80239
Synonyms :

Calculated chemistry of [ 6142-05-8 ]

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 33.48
TPSA : 67.15 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.3 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.18
Log Po/w (WLOGP) : 1.54
Log Po/w (MLOGP) : -0.2
Log Po/w (SILICOS-IT) : 1.67
Consensus Log Po/w : 0.84

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.96
Solubility : 1.5 mg/ml ; 0.011 mol/l
Class : Very soluble
Log S (Ali) : -2.19
Solubility : 0.89 mg/ml ; 0.00652 mol/l
Class : Soluble
Log S (SILICOS-IT) : -0.86
Solubility : 19.0 mg/ml ; 0.139 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.02

Safety of [ 6142-05-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 6142-05-8 ]

* 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 [ 6142-05-8 ]

[ 6142-05-8 ] Synthesis Path-Downstream   1~17

  • 1
  • [ 96-50-4 ]
  • [ 6142-05-8 ]
  • [ 89533-52-8 ]
  • 2
  • [ 6142-05-8 ]
  • [ 17356-08-0 ]
  • [ 19958-82-8 ]
  • 3
  • [ 6142-05-8 ]
  • [ 127099-85-8 ]
  • 1-thiazol-2-yl-biguanide [ No CAS ]
  • 4
  • [ 6142-05-8 ]
  • [ 57-13-6 ]
  • [ 35107-91-6 ]
  • 6
  • [ 124-04-9 ]
  • [ 6142-05-8 ]
  • 5-(Thiazol-2-ylcarbamoyl)-pentanoic acid [ No CAS ]
  • 7
  • [ 1793-07-3 ]
  • [ 6142-05-8 ]
  • 2-(Thiazol-2-ylamino)-benzo[d][1,3]oxazin-4-one [ No CAS ]
  • 8
  • [ 6142-05-8 ]
  • [ 473807-32-8 ]
  • 3-methyl-5-[1-(thiazol-2-yl)pyridin-4(1H)-ylidene]-2-thioxo-1,3-thiazolidin-4-one [ No CAS ]
  • 9
  • [ 40657-29-2 ]
  • [ 6142-05-8 ]
  • (E)-4-ethoxy-1,1,1-tifluoro-4-(1,3-thiazol-2-ylamino)but-3-en-2-one [ No CAS ]
  • 10
  • [ 6142-05-8 ]
  • [ 25602-39-5 ]
YieldReaction ConditionsOperation in experiment
82% With sodium formate; acetic anhydride; In water; benzene; EXAMPLE 5 27.5 grams (0.2 mole) of <strong>[6142-05-8]2-aminothiazole hydrochloride</strong> and 13.6 grams (0.2 mole) of sodium formate were suspended in 100 ml of benzene. There were added dropwise at 40 to 45 C. 41 grams (0.4 mole) of acetic anhydride. The mixture was held at 40 to 45 C. for 2 hours, then cooled to 20 C., washed twice, each time with 50 ml of water and subsequently evaporated to dryness under reduced pressure. There were recovered 21 grams of 2-formylaminothiazole, corresponding to a yield of 82%. The substance had a melting point of 142 to 143 C.
  • 11
  • [ 1023277-63-5 ]
  • [ 6142-05-8 ]
  • [ 1023276-51-8 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In methanol; at 110℃; for 48h; Example 58 8-indan-5-yl-5-oxo-2-[4-(2-pyrrolidin-1-yl-ethyl)-phenylamino]-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid thiazol-2-ylamide (Cpd 131) A solution of 8-indan-5-yl-5-oxo-2-[4-(2-pyrrolidin-1-yl-ethyl)-phenylamino]-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid methyl ester (10 mg) and <strong>[6142-05-8]thiazol-2-ylamine hydrochloride</strong> (20 mg) in 1:1 TEA and MeOH (2 mL) was heated in a sealed tube at 110 C. for 2 days. After cooling, water was added and the solution was directly purified (HPLC, C-18 YMC ODS-A 5mu 30*100 mm, 120 A column at 32 mL/min, 5-100% H2O/MeCN (0.1% TFA v/v) gradient over 10 min.) to provide the title compound (2.5 mg). 1H NMR (TFA salt) (400 MHz, CDCl3) delta (ppm): 9.46 (s, 1H), 8.92 (s, 1H), 7.44-7.35 (m, 3H), 7.30-7.23 (m, 4H), 7.13-7.06 (m, 2H), 3.83 (m, 5H), 3.22-3.13 (m, 2H), 3.01-3.07 (m, 4H), 2.78-2.53 (m, 6H), 2.16-2.20 (m, 4H); Mass Spectrum (LCMS, APCI pos.) Calcd. For: C32H31N7O2S: 577.23; Found: 578.2 (M+H).
  • 12
  • [ 745053-46-7 ]
  • [ 6142-05-8 ]
  • [ 745051-60-9 ]
  • 13
  • [ 1046150-82-6 ]
  • [ 6142-05-8 ]
  • [ 1046150-85-9 ]
  • 14
  • [ 1046150-80-4 ]
  • [ 6142-05-8 ]
  • [ 745053-71-8 ]
  • 15
  • [ 1161733-88-5 ]
  • [ 6142-05-8 ]
  • [ 1397715-50-2 ]
YieldReaction ConditionsOperation in experiment
With nitrogen; Example 13 Preparation of Aminothiazole hydrochloric acid (22) Hydrochloric acid is bubbled through a solution of Boc protected amine (4, 1.4 g, 1.1 mmol) in DCM (20 mL) for thirty min. The reaction mixture is then tightly capped and stirred for thirty minutes after which the reaction mixture is sparged with nitrogen. The mixture loses its gel like appearance. DCM (5 mL) is added to the solution, and HCl gas is bubbled through it for an additional 20 min, followed by nitrogen for 30 min. Crude product (1.32 g) is obtained after concentration as a bright orange solid, and taken on to the next step with no further purification. LCMS: Rt=1.5 min, [M+H]+ 1138.
  • 17
  • [ 7791-25-5 ]
  • [ 1189-71-5 ]
  • [ 6142-05-8 ]
  • boc-sulfonylurea [ No CAS ]
YieldReaction ConditionsOperation in experiment
In pyridine; tert-butyl alcohol; Step 1 To a solution of chlorosulfonylisocyanate (1.35 g, 9.6 mmol) in DCM (50 mL) at 0 C., is added t-BuOH (918 uL, 9.6 mmol) and stirred for 30 min while maintaining temperature at 0 C. To a solution of amine 22 (820 mg, 0.72 mmol) in pyridine (12 mL) is added 0.2 M solution of sulfonyl chloride (1.44 mmol, 0.72 mL). The reaction is stirred for 5 min at 0 C. The solvents were evaporated in vacuo and the solid is purified by basic alumina flash chromatography (gradient elution: 0-10% MeOH/DCM to provide 220 mg of the boc-sulfonylurea. MS (M+H)+1317.
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