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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Chloroaniline | HCID 7812 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 1-hydroxybenzotriazole HOBT | HCID 18366554 | — |
| 反応物 | (3S,4S)-1-((tert-Butoxy)carbonyl)pyrrolidine-3,4-dicarboxylic acid | HCID 69651971 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | trans-(3RS,4RS)-4-(4-Chlorophenylcarbamoyl)-pyrrolidine-1,3-dicarboxylic Acid 1-tert-butyl Ester | HCID 69651960 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07550487B2 |
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| 出典データセット | uspto-grants-2009_06 |
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| ORD ID | ord-1facb16bf5e34afe91c4b2934370f8a8 |
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| 出典メモ | uspto-grants-2009_06 |
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