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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1868518생성일: 2026년 10월 25일

Methanesulfonic acid, 1,1,1-trifluoro-, calcium salt (2:1) → trans-3-[4-(4-Chloro-phenyl)-[1,4]diazepan-1-yl]4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1868518

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참여 물질

역할이름HCID투입량
반응물Methanesulfonic acid, 1,1,1-trifluoro-, calcium salt (2:1)HCID 2734307—
반응물tert-Butyl 6-Oxa-3-azabicyclo(3.1.0)hexane-3-carboxylateHCID 10103880—
반응물1-(4-Chlorophenyl)-1,4-diazepaneHCID 21363820—
용매AcetonitrileHCID 6342—
생성물trans-3-[4-(4-Chloro-phenyl)-[1,4]diazepan-1-yl]4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 5798239243.1%

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온도80 °C

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To a solution of 1-(4-Chloro-phenyl)-[1,4]diazepane (1.00 g, 4.80 mmol) in acetonitrile (10 mL) was added 6-oxa-3-aza-bicyclo[3.1.0]hexane-3-carboxylic acid tert-butyl ester (0.925 g, 5.00 mmol) and calcium(II) trifluoromethanesulfonate (0.676 g, 2.00 mmol). The solution was stirred at 80° C. for 17 hours under nitrogen atmosphere. The reaction was concentrated in vacuo. The residue was diluted with saturated aqueous sodium bicarbonate (50 mL) and extracted with ethyl acetate (3×30 mL). The combined organics were washed with brine, dried over MgSO4, and evaporated. The residue was purified by silica gel chromatography (gradient ethyl acetate to 87:10:3 ethyl acetate:methanol:triethylamine) to yield 0.819 g (41%) of the title compound. ESI-MS m/z: 396 (M+1), FAS method rt: 1.25 min

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07635698B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-13647433be094bb7a7a1432d6a5fb245
출처 메모uspto-grants-2009_12