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HRID 1789494作成日:2026年10月26日

2-(Methylthio)thiazolo[5,4-b]pyridine → 1-acetyl-N-(thiazolo[5,4-b]pyridin-2-yl)-4-piperidinemethanamine

https://huagongshe.com/reaction/1789494

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Methylthio)thiazolo[5,4-b]pyridineHCID 699840—
反応物1-(4-(Aminomethyl)piperidin-1-yl)ethan-1-oneHCID 12687022—
生成物1-acetyl-N-(thiazolo[5,4-b]pyridin-2-yl)-4-piperidinemethanamineHCID 2124157593%

反応条件

温度140 °C

反応手順

A mixture of 11 parts of 1-acetyl-4-piperidinemethanamine and 9 parts of 2-(methylthio)thiazolo[5,4-b]pyridine was stirred and heated for 20 hours at 140° C. The whole was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 13.5 parts (93%) of 1-acetyl-N-(thiazolo[5,4-b]pyridin-2-yl)-4-piperidinemethanamine as a residue (intermediate 51).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04689330
出典データセットuspto-grants-1987_08
ORD IDord-9e71969e97bc4104b9560ff69314f6e6
出典メモuspto-grants-1987_08