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5-AMINO-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID

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Products Intro: Product Name:5-Amino-2-chloropyridine-4-carboxylic acid
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Products Intro: Product Name:5-Amino-2-chloropyridine-4-carboxylic acid
CAS:58483-95-7
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-03361

5-AMINO-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID manufacturers

5-AMINO-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID Basic information
Product Name:5-AMINO-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID
Synonyms:5-AMINO-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID;5-Amino-2-chloropyridine-4-carboxylic acid ,97%;3-amino-6-chloroisonicotinicacid;5-Amino-2-chloro-4-pyridinecarboxylic acid;5-Amino-2-chloropyridine-4-carboxylic acid, 5-Amino-4-carboxy-2-chloropyridine;5-Amino-2-Chloroisonicotinic Acid(WXC01548);5-Amino-2-chloroisonicotinic;4-Pyridinecarboxylic acid, 5-amino-2-chloro-
CAS:58483-95-7
MF:C6H5ClN2O2
MW:172.57
EINECS:687-937-4
Product Categories:Heterocycle-Pyridine series;Pyridine;Carboxylic Acids;Pyridines;Carboxylic Acids
Mol File:58483-95-7.mol
5-AMINO-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID Structure
5-AMINO-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID Chemical Properties
Boiling point 514.4±50.0 °C(Predicted)
density 1.577±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka3.74±0.10(Predicted)
AppearanceOff-white to yellow Solid
InChIInChI=1S/C6H5ClN2O2/c7-5-1-3(6(10)11)4(8)2-9-5/h1-2H,8H2,(H,10,11)
InChIKeyWCZUTMZMEAPPIX-UHFFFAOYSA-N
SMILESC1(Cl)=NC=C(N)C(C(O)=O)=C1
Safety Information
Risk Statements 36/37/38
Safety Statements 22-26-36/37/39
HazardClass IRRITANT
HS Code 29339900
MSDS Information
5-AMINO-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID Usage And Synthesis
Chemical PropertiesBrown powder
Uses3-Amino-6-chloroisonicotinic Acid is a useful synthetic intermediate. It can be used to prepare inhibitors of the EGFr and c-erbB-2. It can also be used to synthesise modulators of GHSr-1a for the treatment of type II diabetes and obesity.
Synthesis
5-[(TERT-BUTOXYCARBONYL)AMINO]-2-CHLOROISONICOTINIC ACID

171178-46-4

5-AMINO-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID

58483-95-7

The general procedure for the synthesis of 5-amino-2-chloropyridine-4-carboxylic acid from 5-tert-butoxycarbonylamino-2-chloropyridine-4-carboxylic acid is as follows: 5-[N-(tert-butoxycarbonyl)amino]-2-chloropyridine-4-carboxylic acid (1.91 g, 7 mmol) was suspended in dichloromethane (200 mL), and trifluoroacetic acid was added slowly dropwise with stirring until the solution became homogeneous (about 5%) 12 mL). The reaction mixture was stirred overnight at room temperature. Subsequently, the reaction mixture was extracted with dilute aqueous ammonia solution and the aqueous phase was acidified with dilute hydrochloric acid to precipitate 5-amino-2-chloropyridine-4-carboxylic acid precipitate (1.05 g, 87% yield). The product was characterized by nuclear magnetic resonance hydrogen spectroscopy (DMSO-d6): δ 9.01 (2H, multiple peaks), 8.03 (1H, single peak), 7.48 (1H, single peak).

References[1] Journal of the Chemical Society - Perkin Transactions 1, 1996, # 18, p. 2221 - 2226
[2] Patent: US5654307, 1997, A
[3] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 11, p. 1401 - 1405
[4] Patent: WO2005/16926, 2005, A1. Location in patent: Page/Page column 115-116; 123
[5] ACS Medicinal Chemistry Letters, 2018, vol. 9, # 3, p. 256 - 261
Tag:5-AMINO-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID(58483-95-7) Related Product Information
3-Amino-2,6-dichloro-isonicotinic acid ethyl ester 5-AMINO-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID 5-AMINO-2-CHLOROPYRIDINE-3-CARBOXYLIC ACID 3-AMINO-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID METHYL ESTER 5-TERT-BUTOXYCARBONYLAMINO-2-CHLORO-NICOTINIC ACID 3-Amino-6-chloropyridine-2-carboxylic acid 2-Amino-5-chloropyridine-3-carboxylic acid 5-Amino-2-chloropyridine 2-Chloropyridine 5-[(TERT-BUTOXYCARBONYL)AMINO]-2-CHLOROISONICOTINIC ACID ETHYL 2-CHLORO-3-CYANO-6-METHYL-5-NITROPYRIDINE-4-CARBOXYLATE 2-amino-6-chloropyridine-4-carboxylic acid 3-amino-5-chloropyridine-2-carboxylic acid 5-Boc-amino-2-chloropyridine-4-carboxylic acid ,97%,5-[N-(TERT-BUTOXYCARBONYL)AMINO]-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID RARECHEM AL BW 1166 6-({2-[bis(propan-2-yl)amino]ethyl}amino)-5-chloropyridine-3-carboxylic acid 6-[(1-{bicyclo[2.2.1]heptan-2-yl}ethyl)amino]-3-chloropyridine-2-carboxylic acid 6-[(4-bromo-3-methylphenyl)amino]-3-chloropyridine-2-carboxylic acid