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HRID 1645353作成日:2026年10月26日

4-(4-{5-[(4-Chloro-benzo[b]thiophene-2-carbonyl)-amino]-pyridin-2-yl}-piperazin-1-yl)-2,2-dimethyl-4-oxo-butyric acid → 4-(4-{4-[(4-Ethoxy-1-ethyl-1H-indole-2-carbonyl)-amino]-phenyl}-piperazin-1-yl)-2,2-dimethyl-4-oxo-butyric acid

https://huagongshe.com/reaction/1645353

反応式

関与物質

役割名称HCID仕込み量
反応物4-(4-{5-[(4-Chloro-benzo[b]thiophene-2-carbonyl)-amino]-pyridin-2-yl}-piperazin-1-yl)-2,2-dimethyl-4-oxo-butyric acidHCID 46207828—
反応物4-ethoxy-1-ethyl-1H-indole-2-carboxylic acid (4-piperazin-4-yl-phenyl)-amideHCID 66775649—
生成物4-(4-{4-[(4-Ethoxy-1-ethyl-1H-indole-2-carbonyl)-amino]-phenyl}-piperazin-1-yl)-2,2-dimethyl-4-oxo-butyric acidHCID 59365196—

反応手順

With a method similar to that used for the preparation of 4-(4-{5-[(4-chloro-benzo[b]thiophene-2-carbonyl)-amino]-pyridin-2-yl}-piperazin-1-yl)-2,2-dimethyl-4-oxo-butyric acid, 4-(4-{4-[(4-ethoxy-1-ethyl-1,1-indole-2-carbonyl)-amino]-phenyl}-piperazin-1-yl)-2,2-dimethyl-4-oxo-butyric acid was prepared from 4-ethoxy-1-ethyl-1H-indole-2-carboxylic acid (4-piperazin-4-yl-phenyl)-amide. LCMS for C29H36N4O5 calcd. (m/e) 520, observed 521 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124766B2
出典データセットuspto-grants-2012_02
ORD IDord-0b56acb3e98b4721bcaadbd2d3f6ed09
出典メモuspto-grants-2012_02