5-broMo-4-Methoxypyridin-2-aMine

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Company Name: Shanghai Jinsheng Pharmaceutical Co., Ltd.  Gold
Tel: 1365-13651960330 13651960330
Email: xiangfeixia@jspharmatech.com
Company Name: PharmaBlock Sciences (Nanjing),Inc.  
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Company Name: NOTA Chemical (Shanghai) Co.,Ltd  
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Company Name: Chiba Pharmaceutical Science and technology Co, Ltd.  
Tel: 0531-81313138 13066006660
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Company Name: Shanghai Famo Bio-chemical Technology Company Ltd.  
Tel: 021-36680027 15821745250
Email: fengqiang@famobiotech.com

5-broMo-4-Methoxypyridin-2-aMine manufacturers

5-broMo-4-Methoxypyridin-2-aMine Basic information
Product Name:5-broMo-4-Methoxypyridin-2-aMine
Synonyms:5-broMo-4-Methoxypyridin-2-aMine;5-BroMo-4-Methoxy-pyridin-2-ylaMine;5-Bromo-4-methoxy-2-pyridinamine hydrobromide;2-Pyridinamine, 5-bromo-4-methoxy-;5-Bromo-4-methoxy-2-pyridinamine;2-Amino-4-methoxy-5-bromopyridine
CAS:1232431-11-6
MF:C6H7BrN2O
MW:203.04
EINECS:
Product Categories:
Mol File:1232431-11-6.mol
5-broMo-4-Methoxypyridin-2-aMine Structure
5-broMo-4-Methoxypyridin-2-aMine Chemical Properties
Boiling point 276.5±35.0 °C(Predicted)
density 1.622±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka5.68±0.24(Predicted)
AppearanceWhite to yellow Solid
InChIInChI=1S/C6H7BrN2O/c1-10-5-2-6(8)9-3-4(5)7/h2-3H,1H3,(H2,8,9)
InChIKeyTWXZYWWOMADXFJ-UHFFFAOYSA-N
SMILESC1(N)=NC=C(Br)C(OC)=C1
Safety Information
HS Code 2933399990
MSDS Information
5-broMo-4-Methoxypyridin-2-aMine Usage And Synthesis
Synthesis
2-Amino-4-methoxypyridine

10201-73-7

5-broMo-4-Methoxypyridin-2-aMine

1232431-11-6

Step 3: Synthesis of 5-bromo-4-methoxy-2-aminopyridine To a solution of 4-methoxy-2-aminopyridine (12.4 g, 100 mmol) in acetonitrile (500 mL) was added N-bromosuccinimide (17.8 g, 100 mmol) in batches, and the reaction was carried out at 0 °C with continuous stirring. After the addition was completed, the reaction mixture was continued to be stirred at room temperature for 1 hour. After completion of the reaction, the solvent was removed by rotary evaporation and the residue was dissolved with dichloromethane. The resulting solution was washed with saturated sodium bicarbonate solution, and the organic phase was dried over anhydrous sodium sulfate and concentrated to afford 5-bromo-4-methoxy-2-aminopyridine (20.3 g, 100% yield), which could be used for subsequent reactions without further purification. Mass spectrum (ESI) m/z: 203.0 [M + H]+.

References[1] Patent: EP2952510, 2015, A1. Location in patent: Paragraph 0143
[2] Tetrahedron Letters, 2014, vol. 55, # 36, p. 5058 - 5061
[3] Patent: US2015/166505, 2015, A1. Location in patent: Paragraph 0428; 0429; 0450
[4] Patent: CN104513257, 2017, B. Location in patent: Paragraph 0411; 0412; 0413
[5] Patent: WO2012/58125, 2012, A1. Location in patent: Page/Page column 139; 140
5-broMo-4-Methoxypyridin-2-aMine Preparation Products And Raw materials
Raw materials2-Amino-4-methoxypyridine-->N-Bromosuccinimide-->Acetonitrile
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