戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 469709作成日:2026年10月26日

Hydrochloric Acid → 1-(3-Chloro-5-trifluoromethyl-pyridin-2-yl)-pyrrolidine-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amide

https://huagongshe.com/reaction/469709

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TriethylamineHCID 8471—
反応物3-Chloro-2-fluoro-5-(trifluoromethyl)pyridineHCID 1268075—
反応物HCID 67455816HCID 67455816—
溶媒EthanolHCID 702—
生成物1-(3-Chloro-5-trifluoromethyl-pyridin-2-yl)-pyrrolidine-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amideHCID 67458346—

反応条件

温度175 °C

反応手順

A microwave reaction vessel is charged with (S)-pyrrolidine-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amide; hydrochloride, 3-chloro-2-fluoro-5-trifluoromethylpyridine, triethylamine and ethanol. The mixture is heated in a microwave reactor at 175° C. for 1 h, maintaining the watts at 60 to keep the reactor from shutting down. The reaction is cooled to room temperature and concentrated in vacuo to afford an oil which is purified by reverse phase preparative HPLC. Product fractions are combined and concentrated in vacuo to afford title compound (64.4 mg). ESI m/z 417 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629157B2
出典データセットuspto-grants-2014_01
ORD IDord-7db17c660c714c0eab8397d3ea7c2c51
出典メモuspto-grants-2014_01