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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40704생성일: 2026년 10월 23일

1-(Methylsulfonyl)piperazine → 3-[4-(4-Methanesulfonylpiperazin-1-yl)phenyl]-3,8-diazabicyclo[3.2.1]-octane-8-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/40704

반응식

참여 물질

역할이름HCID투입량
반응물1-(Methylsulfonyl)piperazineHCID 709161—
반응물2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
반응물Sodium t-butoxideHCID 23676156—
반응물HCID 67413521HCID 67413521—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물3-[4-(4-Methanesulfonylpiperazin-1-yl)phenyl]-3,8-diazabicyclo[3.2.1]-octane-8-carboxylic acid tert-butyl esterHCID 6741346797.9%

반응 단계

3-(4-Bromophenyl)-3,8-diazabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester (0.64 g, 1.7 mmol), 1-methanesulfonylpiperazine (0.43 g, 2.6 mmol), tris-(dibenzylideneacetone)dipalladium (0.069 g, 0.07 mmol), S-Phos (0.11 g, 0.28 mmol), and sodium t-butoxide (0.25 g, 2.6 mmol) are placed in 10 ml of toluene under nitrogen. The reaction medium is stirred at reflux for 1 h 30. After hydrolysis with a saturated aqueous NaHCO3 solution, and extraction with ethyl acetate, the organic phase is washed with a saturated aqueous sodium chloride solution and dried over MgSO4. The crude product obtained is chromatographed on silica gel, elution being carried out with a gradient of methanol/ethyl acetate in dichloromethane ranging from 100/0/0 to 7/2.5/0.5 (dichloromethane/ethyl acetate/methanol). 0.75 g of expected 3-[4-(4-methanesulfonylpiperazin-1-yl)phenyl]-3,8-diazabicyclo[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-1a01cbea3570408d92ecb309f9d6eb9a
출처 메모uspto-grants-2013_09