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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40696생성일: 2026년 10월 24일

3-[4-(4-Methanesulfonylpiperazin-1-yl)phenyl]-8-azabicyclo[3.2.1]oct-2-ene-8-carboxylic acid tert-butyl ester → 3-[4-(4-Methanesulfonylpiperazin-1-yl)phenyl]-8-azabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/40696

반응식

참여 물질

역할이름HCID투입량
반응물3-[4-(4-Methanesulfonylpiperazin-1-yl)phenyl]-8-azabicyclo[3.2.1]oct-2-ene-8-carboxylic acid tert-butyl esterHCID 67413509—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매1-MethoxyethanolHCID 3015637—
생성물3-[4-(4-Methanesulfonylpiperazin-1-yl)phenyl]-8-azabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl esterHCID 6741208291.4%

반응 단계

3-[4-(4-Methanesulfonylpiperazin-1-yl)phenyl]-8-azabicyclo[3.2.1]oct-2-ene-8-carboxylic acid tert-butyl ester (0.83 g, 1.85 mmol) is solubilized in 93 ml of methoxyethanol. Palladium-on-carbon at 10% (0.395 g) is then added. The reaction medium is stirred for 5 h under 30 psi of hydrogen at 25° C. After filtration on Celite® and concentration, 0.76 g of expected 3-[4-(4-methanesulfonylpiperazin-1-yl)phenyl]-8-azabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530477B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-9fb0457a08a0492797d57db8b28d364a
출처 메모uspto-grants-2013_09