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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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Pentafluorobenzoic acid, benzyl esterHCID 517856—
반응물(3S)-(-)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 1514396—
용매AcetonitrileHCID 6342—
생성물(S)-3-(tert-Butoxycarbonylamino)pyrrolidin-1-yl-2,3,5,6-tetrafluorobenzoic acid benzyl esterHCID 8660712863.6%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582627B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-af1fd9678bfe4bb2a9bfe583b721a5f8
출처 메모uspto-grants-2009_09