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HRID 55351作成日:2026年10月26日

(4R)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole-6carboxylic hydrazide → (-)(4R)-6-(5-phenyl-1,3,4-oxadiazol-2yl)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole

https://huagongshe.com/reaction/55351

反応式

関与物質

役割名称HCID仕込み量
反応物(4R)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole-6carboxylic hydrazideHCID 70284014—
溶媒DichloromethaneHCID 6344—
溶媒Trimethyl orthobeznoateHCID 69720—
生成物(-)(4R)-6-(5-phenyl-1,3,4-oxadiazol-2yl)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indoleHCID 22868970163.9%

反応手順

A solution of 0.20 g (0.64 mmol) of (4R)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole-6-carboxylic hydrazide in 2.0 ml of trimethylorthobenzoate was heated at 135° C. under nitrogen for 5 hours. After cooling, the semisolid mixture was dissolved in methylene chloride and the product was extracted into aqueous tartaric acid. The aqueous solution was basified with sodium carbonate and the product was extracted into methylene chloride. Evaporation of the methylene chloride left crystalline product which was then chromatographed over 3 g of silica gel using ethyl acetate as eluent. The product from the column was recrystallized from toluene to give 0.21 g of title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624944
出典データセットuspto-grants-1997_04
ORD IDord-caa328d5a9ed459587c9da23d001ab2e
出典メモuspto-grants-1997_04