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HRID 1773538作成日:2026年10月26日

Phosphorus oxychloride → 3-Methyl-thieno[3,2-b]pyridine-6-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1773538

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus oxychlorideHCID 24813—
反応物3-methyl-6-ethoxycarbonylthieno[3,2-b]pyridin-7(4H)-oneHCID 22574346—
溶媒Ethyl AcetateHCID 8857—
生成物3-Methyl-thieno[3,2-b]pyridine-6-carboxylic acid ethyl esterHCID 5805617383.6%

反応条件

温度150 °C

反応手順

A mixture of 3-methyl-7-oxo-4,7-dihydro-thieno[3,2-b]pyridine-6-carboxylic acid ethyl ester (WO 2003/059878 A2) (1.0 g) and phosphorus oxychloride (3 mL) was heated at 150° C. for 15 minutes in a microwave reactor. The reaction mixture was then cooled and poured into a mixture of ice-water and ethyl acetate. The resulting mixture was stirred for 10 minutes; the organic layer was separated, washed twice with water (50 mL) and with brine, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure. To the solid residue dissolved in a mixture of ethyl acetate and isopropanol (10/1, 55 mL) sodium acetate trihydrate (2.0 g) and palladium hydroxide on carbon (20%, 0.3 g) were added and the resulting mixture was shaken in a Parr apparatus under hydrogen atmosphere (50 PSI) overnight. The reaction mixture was then filtered on a CELITE™ pad, the filtrate was evaporated under reduced pressure and the crude residue was purified by flash chromatography (EtOAc/hexane, 10/90) to afford 0.78 g of 3-methyl-thieno[3,2-b]pyridine-6-carboxylic acid ethyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09255110B2
出典データセットuspto-grants-2016_02
ORD IDord-9ef1aa21ee114950b673689e8c22f943
出典メモuspto-grants-2016_02