Methyl 5-amino-2-chloroisonicotinate

Methyl 5-amino-2-chloroisonicotinate Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: PharmaBlock Sciences (Nanjing),Inc.  
Tel: 025-86918202 4000255188
Email: sales@pharmablock.com
Company Name: Chiba Pharmaceutical Science and technology Co, Ltd.  
Tel: 0531-81313138 13066006660
Email: chibapharm@foxmail.com
Company Name: SynAsst Chemical.  
Tel: 021-60343070
Email:
Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 18317119277
Email: product02@bidepharm.com
Methyl 5-amino-2-chloroisonicotinate Basic information
Product Name:Methyl 5-amino-2-chloroisonicotinate
Synonyms:Methyl 5-aMino-2-chloropyridine-4-carboxylate;Methyl 5-amino-2-chloropyridine-4-carboxylate, 5-Amino-2-chloro-4-(methoxycarbonyl)pyridine;Methyl 5-amino-2-chloroisonicotinate 95%;4-Pyridinecarboxylic acid, 5-amino-2-chloro-, methyl ester;methyl 5-amino-2-chloroisonicotinate
CAS:1073182-59-8
MF:C7H7ClN2O2
MW:186.6
EINECS:
Product Categories:
Mol File:1073182-59-8.mol
Methyl 5-amino-2-chloroisonicotinate Structure
Methyl 5-amino-2-chloroisonicotinate Chemical Properties
storage temp. Keep in dark place,Inert atmosphere,Room temperature
AppearanceLight yellow to yellow Solid
Safety Information
HS Code 2933399990
MSDS Information
Methyl 5-amino-2-chloroisonicotinate Usage And Synthesis
Synthesis
Methanol

67-56-1

5-[(TERT-BUTOXYCARBONYL)AMINO]-2-CHLOROISONICOTINIC ACID

171178-46-4

Methyl 5-amino-2-chloroisonicotinate

1073182-59-8

To a stirred solution of 5-tert-butoxycarbonylamino-2-chloroisonicotinic acid (crude, 8.0 g) in methanol (50 mL) was slowly added concentrated sulfuric acid (5.0 mL). The reaction mixture was heated to reflux and kept at this condition for the reaction overnight. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently concentrated under reduced pressure to remove the solvent. The concentrated residue was diluted with an appropriate amount of water and then neutralized with saturated sodium bicarbonate solution to pH=8. The neutralized aqueous phase was extracted with ethyl acetate (100 mL x2). The organic phases were combined and washed with saturated brine (50 mL), followed by drying with anhydrous sodium sulfate and filtration. The filtrate was evaporated to dryness under reduced pressure and the resulting crude product was purified by silica gel column chromatography.

References[1] Patent: WO2015/200534, A2. Location in patent: Paragraph 00480
[1] Patent: , 2015, . Location in patent: Paragraph 00480
Methyl 5-amino-2-chloroisonicotinate Preparation Products And Raw materials
Raw materialsMethanol-->5-[(tert-Butoxycarbonyl)amino]-2-chloroisonicotinic acid
Preparation Products3-Amino-2-bromo-6-chloro-isonicotinic acid methyl ester
Tag:Methyl 5-amino-2-chloroisonicotinate(1073182-59-8) Related Product Information
5-Amino-2-chloropyridine-4-carboxylic acid 2-Chloro-5-nitro-isonicotinic acid methyl ester 3-Amino-2,6-dichloropyridine-4-carboxylic acid methyl ester 3-Amino-2-chloro-isonicotinic acid methyl ester 4-Pyridinecarboxylic acid, 2-chloro-5-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester 5-aMino-2-chloroisonicotinaldehyde