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HRID 27083作成日:2026年10月23日

Butyric Acid → 5-(4-Butyrylpiperazin-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrrole

https://huagongshe.com/ja/reaction/27083

反応式

関与物質

役割名称HCID仕込み量
反応物Butyric AcidHCID 264—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物RP 35489HCID 3085171—
溶媒DichloromethaneHCID 6344—
生成物5-(4-Butyrylpiperazin-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrroleHCID 1372862767.8%

反応条件

温度20 °C

反応手順

Butyric acid (0.71 g.) is added to a suspension of 6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-5-(piperazin-1-yl)carbonyloxy-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrrole (2.50 g.) and N,N'-dicyclohexyl-carbodiimide (1.67 g.) in anhydrous methylene chloride (50 cc.) and the mixture is stirred for 1 hour at 20° C. After filtering off the dicyclohexylurea formed, washing with methylene chloride (15 cc.) and evaporating the solvent, the residue obtained (3.8 g.) is washed with boiling ethanol (35 cc.) and then recrystallised from a mixture of acetonitrile (110 cc.) and ethanol (11 cc.). 5-(4-Butyrylpiperazin-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrrole (1.95 g.), which melts at 248° C., is thus obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04220646
出典データセットuspto-grants-1980_09
ORD IDord-156be8bfd6dc4e69a16089b33f19744f
出典メモuspto-grants-1980_09