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HRID 236353作成日:2026年10月27日

Pyrrole-2-Carboxylic Acid → beta-Oxo-alpha-(phenylcarbamoyl)-beta-(2-pyrrolyl)-propionitrile

https://huagongshe.com/reaction/236353

反応式

関与物質

役割名称HCID仕込み量
反応物Pyrrole-2-Carboxylic AcidHCID 12473—
反応物Acetamide, 2-cyano-N-phenyl-HCID 69296—
反応物Diethyl cyanophosphonateHCID 76257—
反応物Potassium tert-butoxideHCID 23665647—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物beta-Oxo-alpha-(phenylcarbamoyl)-beta-(2-pyrrolyl)-propionitrileHCID 13370089—

反応手順

to a solution of 1.6 g of α-cyanoacetanilide in 10 ml of dimethylformamide is added 3.4 g of potassium t-butoxide. The stirred cooled suspension is treated with a solution of 1.1 g of pyrrole-2-carboxylic acid and 1.4 ml of diethyl phosphorocyanidate in 6 ml of dimethylformamide. After standing for one half hour, solution is treated with 80 ml of cold water, filtered and acidified with 6N hydrochloric acid. The suspended product is collected, washed with water, dried, and dissolved in ethyl acetate. The ethyl acetate solution is filtered and evaporated to dryness. Recrystallization from ether-ethanol yields β-oxo-α-(phenylcarbamoyl)-β-(2-pyrrolyl)-propionitrile of Example 1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04644010
出典データセットuspto-grants-1987_02
ORD IDord-b292133de2964c528d6c4406c7bce408
出典メモuspto-grants-1987_02