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2-Bromo-6-chloropyridin-3-amine

2-Bromo-6-chloropyridin-3-amine Suppliers list
Company Name: Shanghai YuYuan Pharmaceutical Co., Ltd.  Gold
Tel: 13052276172
Email: product@yuyuanpharm.com
Company Name: shanghaiaoderuikanglimitedcompany  Gold
Tel: 18902198068 18912886236
Email: akslichenglong@163.com
Company Name: Changzhou Jienuo Pharmaceutical Technology Co., Ltd  Gold
Tel: 13915093723
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Company Name: Energy Chemical  
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Company Name: Wuhan Chemwish Technology Co., Ltd  
Tel: 86-027-67849912
Email: sales@chemwish.com

2-Bromo-6-chloropyridin-3-amine manufacturers

2-Bromo-6-chloropyridin-3-amine Basic information
Product Name:2-Bromo-6-chloropyridin-3-amine
Synonyms:2-Bromo-6-chloropyridin-3-amine;3-Amino-2-bromo-6-chloropyridine;3-AMINO-6-CHLORO-2-BROMOPYRIDINE;2-Bromo-6-chloro-3-pyridinamine;2-Bromo-6-chloro-pyridin-3-ylamine;3-Pyridinamine, 2-bromo-6-chloro-;2-Bromo-6-chloropyridin-3-amine ISO 9001:2015 REACH;2-bromo-3-amino-6-chloropyridine
CAS:1050501-88-6
MF:C5H4BrClN2
MW:207.46
EINECS:
Product Categories:
Mol File:1050501-88-6.mol
2-Bromo-6-chloropyridin-3-amine Structure
2-Bromo-6-chloropyridin-3-amine Chemical Properties
Boiling point 330.3±37.0 °C(Predicted)
density 1.834
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka-0.12±0.10(Predicted)
AppearanceLight brown to brown Solid
InChIInChI=1S/C5H4BrClN2/c6-5-3(8)1-2-4(7)9-5/h1-2H,8H2
InChIKeyOPKKXWUGXHSFQI-UHFFFAOYSA-N
SMILESC1C=C(N)C(Br)=NC=1Cl
Safety Information
HS Code 2933399990
MSDS Information
2-Bromo-6-chloropyridin-3-amine Usage And Synthesis
Uses2-Bromo-6-chloro-3-pyridinamine is a reactant used in the synthesis of kilogram quantities of an akt Kinase inhibitor. It is mainly used as starting material for the production of many pharmaceutical compounds.
Synthesis
5-Amino-2-chloropyridine

5350-93-6

2-Bromo-6-chloropyridin-3-amine

1050501-88-6

Step 1: Synthesis of 2-bromo-6-chloropyridin-3-amine Bromine (24.86 g, 155.57 mmol) was slowly added to a solution of acetic acid (383 mL) containing 6-chloropyridin-3-amine (20.00 g, 155.57 mmol) and sodium acetate (25.52 g, 311.14 mmol). The reaction mixture was stirred at room temperature for 1 hour. Subsequently, the acetic acid was removed by rotary evaporator. The residue was dissolved in ethyl acetate (EtOAc) and washed sequentially with saturated aqueous sodium carbonate (Na2CO3) solution, water and brine. The organic layer was dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated to afford the target product 2-bromo-6-chloropyridin-3-amine (32.20 g, 99.8% yield). Mass spectrometry analysis showed m/z = 206.96 ([M+H]+), which is consistent with the isotopic distribution pattern of Cl and Br.

References[1] Patent: WO2012/80450, 2012, A1. Location in patent: Page/Page column 25
[2] Patent: WO2013/186335, 2013, A1. Location in patent: Page/Page column 87
[3] Patent: WO2013/186333, 2013, A1. Location in patent: Page/Page column 102
[4] Patent: WO2014/60411, 2014, A1. Location in patent: Page/Page column 56
[5] Patent: US2015/111868, 2015, A1. Location in patent: Paragraph 0856; 0857
2-Bromo-6-chloropyridin-3-amine Preparation Products And Raw materials
Raw materials5-Amino-2-chloropyridine-->Sodium carbonate-->Sodium chloride-->Ethyl acetate-->Water
Preparation Productstert-butyl 2-broMo-6-chloropyridin-3-ylcarbaMate-->5-Chloro-1H-pyrrolo[3,2-b] pyridine
Tag:2-Bromo-6-chloropyridin-3-amine(1050501-88-6) Related Product Information
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