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145325-40-2

145325-40-2 Structure

145325-40-2 Structure
IdentificationBack Directory
[Name]

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

145325-40-2
[Synonyms]

Methyl 4-broMothieno[2,3-...
Methyl 4-bromothieno[2,3-c]pyridine-2-carboxyla
METHYL 4-BROMOTHIENO[2,3-C]PYRIDINE-2-CARBOXYLATE
4-BROMOTHIENO[2,3-C]PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER
Thieno[2,3-c]pyridine-2-carboxylic acid, 4-broMo-, Methyl ester
[Molecular Formula]

C9H6BrNO2S
[MDL Number]

MFCD08275124
[MOL File]

145325-40-2.mol
[Molecular Weight]

272.12
Chemical PropertiesBack Directory
[Boiling point ]

372.7±37.0 °C(Predicted)
[density ]

1.697±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

1.21±0.40(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P280-P305+P351+P338-P310
Spectrum DetailBack Directory
[Spectrum Detail]

4-BROMOTHIENO[2,3-C]PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER(145325-40-2)1HNMR
Hazard InformationBack Directory
[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
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