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HRID 1987171作成日:2026年10月26日

4-Chloroaniline → trans-(3RS,4RS)-4-(4-Chlorophenylcarbamoyl)-pyrrolidine-1,3-dicarboxylic Acid 1-tert-butyl Ester

https://huagongshe.com/reaction/1987171

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChloroanilineHCID 7812—
反応物DiisopropylethylamineHCID 81531—
反応物1-hydroxybenzotriazole HOBTHCID 18366554—
反応物(3S,4S)-1-((tert-Butoxy)carbonyl)pyrrolidine-3,4-dicarboxylic acidHCID 69651971—
溶媒AcetonitrileHCID 6342—
生成物trans-(3RS,4RS)-4-(4-Chlorophenylcarbamoyl)-pyrrolidine-1,3-dicarboxylic Acid 1-tert-butyl EsterHCID 69651960—

反応条件

温度25 °C

反応手順

Compound 1c (2.25 g; 9 mmol) is suspended in acetonitrile (30 ml) and N,N-diisopropyl ethyl amin (3.03 ml; 17 mmol) is added at 25° C. After 20 min a clear solution is obtained and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride EDCI (2.0 g; 10 mmol) and 1-hydroxybenzotriazole HOBt (1.41 g; 10 mmol) is added. After stirring for 30 min at 25° C. 4-chloroaniline (1.11 g; 9 mmol) is added to the reaction mixture. The mixture is stirred for 18 h at 25° C., evaporated to dryness and dissolved in ethyl acetate (100 ml). The organic phase is washed with 0.1 N HCl (2×100 ml), water and brine and dried over Na2SO4. The organic phase is filtered and the filtrate is evaporated to dryness. Yield: 1.08 g (33.7%), ESI-MS: m/z=368 [M−H]−, Cl-pattern

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07550487B2
出典データセットuspto-grants-2009_06
ORD IDord-1facb16bf5e34afe91c4b2934370f8a8
出典メモuspto-grants-2009_06