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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71685생성일: 2026년 10월 25일

Diisopropylethylamine → 2-[1-(4-Bromo-phenyl)-1-ethoxycarbonyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/71685

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1-((Tert-butoxy)carbonyl)pyrrolidine-3-carboxylic acidHCID 2760529—
반응물Ethyl 2-amino-2-(4-bromophenyl)propanoateHCID 3494252—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
용매DimethylformamideHCID 6228—
생성물2-[1-(4-Bromo-phenyl)-1-ethoxycarbonyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 6662044958.8%

반응 단계

N,N-diisopropylethylamine (4.1 mL, 23.6 mmol) was added dropwise to a mixture of pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester (0.7 g, 3.2 mmol), HATU (1.2 g, 3.2 mmol) and 2-amino-2-(4-bromo-phenyl)-propionic acid ethyl ester (0.8 g, 2.9 mmol) in DMF (20 mL), and stirred at ambient condition for 3 hours. Most of the volatile component was removed in vacuo, and the resulting residue was dissolved in ethyl acetate (150 mL), washed with water and brine, dried over Na2SO4, filtered and concentrated in vacuo. The obtained residue was purified by flash chromatography to provide the desired product as a colorless oil (0.8 g, 58%). m/z 490.9, 492.9 (M+Na)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822430B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d26cd7743c354e00a867d948ff49cd64
출처 메모uspto-grants-2014_09