돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1992465생성일: 2026년 10월 25일

1-(Benzenesulfonyl)piperazine → (4-Benzenesulfonyl-piperazin-1-yl)-[5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanone

https://huagongshe.com/reaction/1992465

반응식

참여 물질

역할이름HCID투입량
반응물1-(Benzenesulfonyl)piperazineHCID 808712—
반응물[5-(4-Isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-(4-methanesulfonyl-piperazin-1-yl)-methanoneHCID 68538245—
생성물(4-Benzenesulfonyl-piperazin-1-yl)-[5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanoneHCID 6853584692%

반응 단계

The title compound was synthesized in analogy to example 1, from 5-(4-isopropyl-piperazine-1-carbonyl)-1H-indole-2-carboxylic acid hydrochloride (example 1, intermediate b) and 1-benzenesulfonyl-piperazine to afford the desired product as a light-brown foam (92%). MS (ISP): 524.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07648979B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-8f7edb21f40146ef83d62e0a66e79c67
출처 메모uspto-grants-2010_01