Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pyrrolidine → N-(2-amino-5-bromophenyl)pyrrolidine-1-carboxamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pyrrolidine | HCID 31268 | — |
| 반응물 | Triphosgene | HCID 94429 | — |
| 반응물 | 5-Bromo-2-nitroaniline | HCID 5314766 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(2-amino-5-bromophenyl)pyrrolidine-1-carboxamide | HCID 86712537 | 34.4% |
반응 단계
To a solution of 5-bromo-2-nitroaniline (1 g, 4.61 mmol) in dichloromethane (15 mL) were added TEA (8.35 mL, 59.9 mmol, 1.3 eq.) and triphosgene (1.37 g, 4.61 mmol, 1 equiv.) at 0° C. The mixture was stirred for three hours at room temperature and the pyrrolidine (0.39 g, 5.53 mmol, 1.2 equiv.) was added slowly. The reaction was stirred for an additional two hours. The reaction crude was diluted with dichloromethane and washed with water and brine. The organic layers were dried over MgSO4, filtered and evaporated. The residue was purified by column chromatography on eluting ethyl acetate and hexane to allow N-(2-amino-5-bromophenyl)pyrrolidine-1-carboxamide (0.45 g, 31% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09447030B2 |
| 출처 데이터셋 | uspto-grants-2016_09 |
| ORD ID | ord-bc741af4a26c43ffb06e37aa6e257499 |
| 출처 메모 | uspto-grants-2016_09 |