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HRID 635875作成日:2026年10月26日

Benzaldehyde → 3-[3-(2,3-Dimethylimidazo[2,1-b]thiazol-5-yl)-3-oxo-1-propenyl]phenyl-4-methylbenzenesulfonamide

https://huagongshe.com/reaction/635875

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物o-Toluenesulfonyl chlorideHCID 8623—
反応物Benzaldehyde, 3-amino-HCID 74366—
反応物m-ToluenesulphonamideHCID 74697—
反応物2,3-Dimethylimidazo[2,1-b]thiazol-5-yl ethanoneHCID 21256445—
生成物3-[3-(2,3-Dimethylimidazo[2,1-b]thiazol-5-yl)-3-oxo-1-propenyl]phenyl-4-methylbenzenesulfonamideHCID 86756428—

反応手順

1-(2,3-Dimethylimidazo[2,1-b]-thiazol-5-yl ethanone (Formula N′-1), 0.97 g, was condensed with the 3-toluensulfonamide of benzaldehyde, m.p. 126-127°, prepared from toluene sulfonyl chloride and 3-aminobenzaldehyde, according to non-critical modifications of PREPARATION 15 to provide pure (E)-N-[3-[3-(2,3-Dimethylimidazo[2,1-b]thiazol-5-yl)-3-oxo-1-propenyl]phenyl-4-methylbenzenesulfonamide, m.p. 236-237°, Formula N′-2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06191124B1
出典データセットuspto-grants-2001_02
ORD IDord-ed899c7d24cd4a589abc1bab3ad8f41e
出典メモuspto-grants-2001_02