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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44452생성일: 2026년 10월 23일

Diisopropylethylamine → (S)-benzyl 2-(4-(tert-butoxycarbonylamino)phenylcarbamoyl)pyrrolidine-1-carboxylate

https://huagongshe.com/ko/reaction/44452

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Benzyloxycarbonyl-L-prolineHCID 101987—
반응물tert-Butyl (4-aminophenyl)carbamateHCID 688611—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물(S)-benzyl 2-(4-(tert-butoxycarbonylamino)phenylcarbamoyl)pyrrolidine-1-carboxylateHCID 5939612270%

반응 단계

To a solution of Carbobenzyloxy-L-proline (0.20 g, 0.80 mmol) and HATU (0.32 g, 0.84 mmol) in DMSO (6 mL) was added diisopropylethylamine (0.42 mL, 2.41 mmol) followed by tert-buty-4-aminophenylcarbamate (0.175 g, 0.82 mmol). The solution was stirred at ambient temperature for two hours, then diluted with water and the solid product was filtered off and purified by combi-flash 12 g column, eluting with 0-20% ethyl acetate in dichloromethane to give a solid (0.245 g, 70%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541424B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-4a825562167a45caa179f859a95ce40d
출처 메모uspto-grants-2013_09