(6-AMino-5-broMo-pyridin-3-yl)-Methanol

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Company Name: Shanghai Sunway Pharmaceutical Technology Co., Ltd  
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Email: hxzheng@sunwaypharm.cn
Company Name: Hunan Hui Bai Shi Biotechnology Co., Ltd.  
Tel: 0731-85526065 13308475853
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Company Name: SuZhou ShiYa Biopharmaceuticals, Inc.  
Tel: 86(512)5235 8471 17715136450
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Company Name: Cochemical Ltd.  
Tel: 029-86115547 17791676824
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Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 18317119277
Email: product02@bidepharm.com

(6-AMino-5-broMo-pyridin-3-yl)-Methanol manufacturers

(6-AMino-5-broMo-pyridin-3-yl)-Methanol Basic information
Product Name:(6-AMino-5-broMo-pyridin-3-yl)-Methanol
Synonyms:6-AMino-5-broMopyridine-3-Methanol;3-Pyridinemethanol, 6-amino-5-bromo-;(6-AMino-5-broMo-pyridin-3-yl)-Methanol
CAS:1027785-19-8
MF:C6H7BrN2O
MW:203.04
EINECS:
Product Categories:
Mol File:1027785-19-8.mol
(6-AMino-5-broMo-pyridin-3-yl)-Methanol Structure
(6-AMino-5-broMo-pyridin-3-yl)-Methanol Chemical Properties
Boiling point 344.4±37.0 °C(Predicted)
density 1.766±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka13.22±0.10(Predicted)
AppearanceLight brown to brown Solid
Safety Information
MSDS Information
(6-AMino-5-broMo-pyridin-3-yl)-Methanol Usage And Synthesis
Synthesis
ETHYL 2-AMINO-3-BROMO-5-PYRIDINECARBOXYLATE

850429-51-5

(6-AMino-5-broMo-pyridin-3-yl)-Methanol

1027785-19-8

General procedure for the synthesis of (6-amino-5-bromopyridin-3-yl)methanol from ethyl 6-amino-5-bromonicotinate: A) Ethyl 6-amino-5-bromonicotinate (2.31 g, 10 mmol) was dissolved in tetrahydrofuran (20 mL) at room temperature and lithium aluminum hydride (LAH, 10 mL, 1 M solution in tetrahydrofuran) was added slowly and dropwise. The reaction mixture was stirred for 1 h. The reaction was quenched by careful addition of water (0.2 mL). The resulting precipitate was collected by filtration and washed with ethyl acetate. The filtrate was concentrated under reduced pressure to give (6-amino-5-bromopyridin-3-yl)methanol (2.0 g, 99% yield) as a white solid. The product was confirmed by LC/MS analysis showing (M + H)+ = 203, 205 (ratio 1:1).1H NMR (CD3OD, 300 MHz) data were as follows: δ 7.79 (s, 1H), 7.67 (s, 1H), 4.35 (br s, 2H).

References[1] Patent: WO2008/60907, 2008, A2. Location in patent: Page/Page column 34-35
(6-AMino-5-broMo-pyridin-3-yl)-Methanol Preparation Products And Raw materials
Raw materialsEthyl 2-amino-3-bromo-5-pyridinecarboxylate-->Tetrahydrofuran-->Lithium Aluminum Hydride
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