3-Bromo-2-chloro-5-nitro-pyridin-4-amine

3-Bromo-2-chloro-5-nitro-pyridin-4-amine Suppliers list
Company Name: Jiaxing Rich Biological Technology Co., Ltd.  
Tel: 0573-11111111-1111 18969316891
Email: richmol@163.com
Company Name: SuZhou ShiYa Biopharmaceuticals, Inc.  
Tel: 0512-0512-52358471 17715136450
Email: sales@shiyabiopharm.com
Company Name: Amadis Chemical Company Limited  
Tel: 571-89925085
Email: sales@amadischem.com
Company Name: Shanghai Pingguo Pharmaceutical Co., Ltd.  
Tel: 021-20432229
Email: 2412110556@qq.com
Company Name: Aikon International Limited  
Tel: 025-66061636 19370895928
Email: qqyang@aikonchem.com

3-Bromo-2-chloro-5-nitro-pyridin-4-amine manufacturers

3-Bromo-2-chloro-5-nitro-pyridin-4-amine Basic information
Product Name:3-Bromo-2-chloro-5-nitro-pyridin-4-amine
Synonyms:4-Bromo-5-chloro-2-nitropyridin-3-amine;4-Pyridinamine, 3-bromo-2-chloro-5-nitro-;3-Bromo-2-chloro-5-nitro-pyridin-4-amine
CAS:1268521-33-0
MF:C5H3BrClN3O2
MW:252.45
EINECS:200-589-5
Product Categories:
Mol File:1268521-33-0.mol
3-Bromo-2-chloro-5-nitro-pyridin-4-amine Structure
3-Bromo-2-chloro-5-nitro-pyridin-4-amine Chemical Properties
Boiling point 390.3±37.0 °C(Predicted)
density 2.020±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka-1.46±0.50(Predicted)
AppearanceOff-white to yellow Solid
Safety Information
MSDS Information
3-Bromo-2-chloro-5-nitro-pyridin-4-amine Usage And Synthesis
Synthesis
4-AMINO-3-BROMO-2-CHLOROPYRIDINE

215364-85-5

3-BROMO-2-CHLORO-5-NITRO-PYRIDIN-4-AMINE

1268521-33-0

Potassium nitrate (4.87 g, 48.20 mmol) was slowly added to a stirred solution of 3-bromo-2-chloropyridin-4-amine (5.00 g, 24.10 mmol) in concentrated sulfuric acid (36 mL) at about 5 °C. The reaction mixture was gradually warmed to room temperature and stirred continuously for 20 hours. Subsequently, the reaction mixture was slowly poured into crushed ice (~400 mL) and a light yellow precipitate precipitated. The precipitate was collected by filtration and washed with plenty of water. The resulting solid was dried under reduced pressure and added in batches to concentrated sulfuric acid (30 mL), maintaining the temperature at about 5 °C. The reaction mixture was heated to 90 °C and stirred for 2 hours before being cooled to room temperature and allowed to stand for 18 hours. The reaction mixture was again poured into crushed ice (about 400 mL) and a precipitate was precipitated, collected by filtration and washed with cold water. The solid was dissolved in a mixed solvent of methanol and ethyl acetate, and the solution was dried over anhydrous sodium sulfate and concentrated in vacuum to give 3-bromo-2-chloro-5-nitropyridin-4-amine (5.20 g, 85% yield) as a pale orange solid.LCMS (Method I, ESI): retention time = 2.79 min, [M+H]+ = 251.9/253.9/255.9; 1H NMR (400 MHz, DMSO-d6): δ 8.86 (1H, s).

References[1] Patent: WO2013/7765, 2013, A1. Location in patent: Page/Page column 185-186
3-Bromo-2-chloro-5-nitro-pyridin-4-amine Preparation Products And Raw materials
Raw materials2-Chloro-5-nitropyridin-4-amine-->4-Amino-3-bromo-2-chloropyridine
Tag:3-Bromo-2-chloro-5-nitro-pyridin-4-amine(1268521-33-0) Related Product Information