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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1786459생성일: 2026년 10월 26일

tert-Butyl piperazine-1-carboxylate → [6-Bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(4-cyclopropanesulfonyl-piperazin-1-yl)-methanone

https://huagongshe.com/reaction/1786459

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물Cyclopropanesulfonyl chlorideHCID 2760919—
반응물1-(Cyclopropylsulfonyl)piperazineHCID 45496790—
반응물6-bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indole-2-carboxylic acid hydrochlorideHCID 67017930—
생성물[6-Bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(4-cyclopropanesulfonyl-piperazin-1-yl)-methanoneHCID 6856678162%

반응 단계

The title compound was synthesized in analogy to example 1, from 6-bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indole-2-carboxylic acid hydrochloride (example 1, intermediate a) and cyclopropylsulfonyl-piperazine (prepared in analogy to International Patent Application Publ. No. WO 2003/064413 by using cyclopropylsulfonyl chloride and tert-butyl 1-piperazinecarboxylate) to afford the title compound as a light-yellow solid (62%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07507736B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-2200d6b7e9f94cecbba6c389b32d518b
출처 메모uspto-grants-2009_03