Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 729371생성일: 2026년 10월 26일
Triethylamine → (S)-3-(tert-Butoxycarbonylamino)pyrrolidin-1-yl-2,3,5,6-tetrafluorobenzoic acid benzyl ester
https://huagongshe.com/reaction/729371
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Pentafluorobenzoic acid, benzyl ester | HCID 517856 | — |
| 반응물 | (3S)-(-)-3-(tert-Butoxycarbonylamino)pyrrolidine | HCID 1514396 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | (S)-3-(tert-Butoxycarbonylamino)pyrrolidin-1-yl-2,3,5,6-tetrafluorobenzoic acid benzyl ester | HCID 86607128 | 63.6% |
반응 단계
A solution of 2,3,4,5,6-pentafluorobenzoic acid benzyl ester (Example 1d, 8.05 g, 26.6 mmol), triethylamine (26 mL, 186 mmol), and (S)-pyrrolidin-3-yl-carbamic acid tert-butyl ester (5.6 g, 30 mmol) in acetonitrile (150 mL) is stirred at room temperature for 24 hours. The solvent is removed under vacuum and the residue dissolved in chloroform, washed with NaHCO3 and then brine, dried over Na2SO4, filtered, and concentrated in vacuo to afford a solid. The solid is then purified by column chromatography (1:1:6 ethyl acetate/chloroform/hexanes) to yield the title compound as a solid (7.92 g). 1H NMR (CDCl3): δ 7.48-7.30 (m, 5H, 5.35 (s, 2H), 4.77-4.50 (m, 1H), 4.37-4.19 (m, 1H), 4.01-3.63 (m, 3H), 3.59-3.46 (m, 1H), 2.29-2.09 (m, 1H), 2.01-1.82 (m, 1H), 1.45 (s, 9H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07582627B2 |
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| 출처 데이터셋 | uspto-grants-2009_09 |
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| ORD ID | ord-af1fd9678bfe4bb2a9bfe583b721a5f8 |
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| 출처 메모 | uspto-grants-2009_09 |
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