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HRID 1363755作成日:2026年10月26日

m-Aminoacetanilide → 3-{2-[3-(3-Acetylamino-phenyl)-3-cyclopentylmethyl-ureido]-thiazol-5-ylsulfanyl}-propionic acid

https://huagongshe.com/reaction/1363755

反応式

関与物質

役割名称HCID仕込み量
反応物m-AminoacetanilideHCID 7604—
反応物CyclopentanecarbaldehydeHCID 70106—
反応物Ethyl 3-[(2-amino-1,3-thiazol-5-YL)sulfanyl]propanoateHCID 57481428—
反応物{2-[3-Cyclopentylmethyl-3-(3,4-difluoro-phenyl)-ureido]-thiazol-4-yl}-acetic acidHCID 57668246—
反応物3-{2-[3-(3-Acetylamino-phenyl)-3-cyclopentylmethyl-ureido]-thiazol-5-ylsulfanyl}-propionic acid ethyl esterHCID 86629888—
生成物3-{2-[3-(3-Acetylamino-phenyl)-3-cyclopentylmethyl-ureido]-thiazol-5-ylsulfanyl}-propionic acidHCID 57668415—

反応手順

The title compound was prepared via 3-{2-[3-(3-acetylamino-phenyl)-3-cyclopentylmethyl-ureido]-thiazol-5-ylsulfanyl}-propionic acid ethyl ester in a similar manner as described for the synthesis of {2-[3-cyclopentylmethyl-3-(3,4-difluoro-phenyl)-ureido]-thiazol-4-yl}-acetic acid, using N-(3-amino-phenyl)-acetamide, cyclopentanecarbaldehyde and 3-(2-amino-thiazol-5-ylsulfanyl)-propionic acid ethyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07884210B2
出典データセットuspto-grants-2011_02
ORD IDord-919d525567a44db28b19af69a5043862
出典メモuspto-grants-2011_02