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4-Bromothieno[2,3-c]pyridine-2-carboxylic acid methyl ester

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4-Bromothieno[2,3-c]pyridine-2-carboxylic acid methyl ester manufacturers

4-Bromothieno[2,3-c]pyridine-2-carboxylic acid methyl ester Basic information
Product Name:4-Bromothieno[2,3-c]pyridine-2-carboxylic acid methyl ester
Synonyms:METHYL 4-BROMOTHIENO[2,3-C]PYRIDINE-2-CARBOXYLATE;Thieno[2,3-c]pyridine-2-carboxylic acid, 4-broMo-, Methyl ester;Methyl 4-broMothieno[2,3-...;Methyl 4-bromothieno[2,3-c]pyridine-2-carboxyla;4-Bromothieno[2,3-c]pyridine-2-carboxylic acid methyl ester
CAS:145325-40-2
MF:C9H6BrNO2S
MW:272.12
EINECS:
Product Categories:Building Blocks;Thieno[x,x-y]pyridine
Mol File:145325-40-2.mol
4-Bromothieno[2,3-c]pyridine-2-carboxylic acid methyl ester Structure
4-Bromothieno[2,3-c]pyridine-2-carboxylic acid methyl ester Chemical Properties
Boiling point 372.7±37.0 °C(Predicted)
density 1.697±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka1.21±0.40(Predicted)
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
4-Bromothieno[2,3-c]pyridine-2-carboxylic acid methyl ester Usage And Synthesis
Synthesis
3,5-Dibromopyridine-4-carboxaldehyde

70201-42-2

Methyl thioglycolate

2365-48-2

4-BROMOTHIENO[2,3-C]PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER

145325-40-2

Under nitrogen atmosphere, 3,5-dibromopyridine-4-carboxaldehyde (80 g, 303 mmol) and cesium carbonate (98 g, 302 mmol) were sequentially added to a 2L round-bottomed flask containing tetrahydrofuran (1.3 L). Methyl mercaptoacetate (32 g, 302 mmol) was then added and the reaction mixture was stirred at 60 °C overnight. After completion of the reaction, it was cooled to room temperature and extracted by adding ethyl acetate. The organic layer was washed sequentially with water, saturated aqueous sodium bicarbonate solution and brine, dried over anhydrous sodium sulfate and filtered to give a white solid crude product. The crude product was purified by recrystallization from ethyl acetate to finally obtain methyl 4-bromothieno[2,3-C]pyridine-2-carboxylate (60 g, 73% yield).

References[1] Patent: WO2013/127266, 2013, A1. Location in patent: Page/Page column 135
[2] Patent: WO2013/127267, 2013, A1. Location in patent: Page/Page column 86; 87
[3] Patent: WO2013/127268, 2013, A1. Location in patent: Page/Page column 64; 65
[4] Patent: WO2013/130935, 2013, A1. Location in patent: Paragraph 0188
[5] Journal of Heterocyclic Chemistry, 2008, vol. 45, # 1, p. 91 - 96
4-Bromothieno[2,3-c]pyridine-2-carboxylic acid methyl ester Preparation Products And Raw materials
Raw materials3,5-Dibromopyridine-4-carboxaldehyde-->Methyl thioglycolate-->Tetrahydrofuran-->Cesium carbonate
Tag:4-Bromothieno[2,3-c]pyridine-2-carboxylic acid methyl ester(145325-40-2) Related Product Information
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