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HRID 14745作成日:2026年10月24日

Tert-butyl 3-oxopyrrolidine-1-carboxylate → 3-[3-(2-Chloro-pyrimidin-4-yl)-phenylamino]-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ja/reaction/14745

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
反応物3-(2-Chloropyrimidin-4-yl)anilineHCID 59341023—
生成物3-[3-(2-Chloro-pyrimidin-4-yl)-phenylamino]-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 8660324670%

反応手順

Intermediate 6 was coupled with 3-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester following procedure J. The product was purified on silica gel using 1:1 ethyl acetate:hexanes as eluent. Yield: 70%. LC-MS showed the product had the expected M+H+ of 375.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732444B2
出典データセットuspto-grants-2010_06
ORD IDord-1fc235b6f85a43b4a99287ff419e95a2
出典メモuspto-grants-2010_06