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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 603208생성일: 2026년 10월 25일

Diisopropylethylamine → Tert-butyl 3-[(4-{[(3,4-dichlorophenyl)amino]carbonyl}piperazin-1-yl)carbonyl]pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/603208

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물N-(3,4-Dichlorophenyl)piperazine-1-carboxamideHCID 16775732—
반응물3-carboxy-N-boc-prolineHCID 67220720—
용매DimethylformamideHCID 6228—
생성물Tert-butyl 3-[(4-{[(3,4-dichlorophenyl)amino]carbonyl}piperazin-1-yl)carbonyl]pyrrolidine-1-carboxylateHCID 5765670799%

반응 단계

To a stirred solution of N-(3,4-dichlorophenyl)piperazine-1-carboxamide (2.00 g, 7.30 mmol) in DMF (150 ml) was added DIPEA (3.8 ml, 21.9 mmol), 3-carboxy-N-boc-proline (Arch Corporation) (1.727 g, 8.02 mmol) and HATU (3.051 g, 8.02 mmol) and the reaction stirred at ambient temperature for overnight (convenience). The solvents were then removed under reduced pressure. The resulting gum was then partitioned between EtOAc and water, extracted, the organic phase washed with saturated sodium bicarbonate solution and evaporated to dryness. The resulting foam was then purified on Isco™ Companion (40 g column:EtOAc) to give the product tert-butyl 3-[(4-{[(3,4-dichlorophenyl)amino]carbonyl}piperazin-1-yl)carbonyl]pyrrolidine-1-carboxylate as a pale yellow foam (3.396 g, 7.20 mmol, 99%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906645B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-1294b04125fd4428a472f6ba4569c2c3
출처 메모uspto-grants-2011_03