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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1632870생성일: 2026년 10월 27일

Water → p-Nitrobenzyl(5RS,6SR)-3-[(Z)-2-Acetamidoethenylthio]-6-[(1RS)-1-p-nitrobenzyloxycarbonyloxyethyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate

https://huagongshe.com/reaction/1632870

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물p-Nitrobenzyl(5RS,6SR)-6-[(1RS)-1-p-nitrobenzyloxycarbonyloxyethyl]-3-(2-pyrimidylsulphinyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylateHCID 20442568—
촉매Benzylhexadecyldimethylammonium chlorideHCID 31202—
용매DichloromethaneHCID 6344—
생성물p-Nitrobenzyl(5RS,6SR)-3-[(Z)-2-Acetamidoethenylthio]-6-[(1RS)-1-p-nitrobenzyloxycarbonyloxyethyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylateHCID 8872375752%

반응 단계

p-Nitrobenzyl(5RS,6SR)-6-[(1RS)-1-p-nitrobenzyloxycarbonyloxyethyl]-3-(2-pyrimidylsulphinyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (230 mg) in dichloromethane (25 ml) was treated with benzyldimethyl-n-hexadecylammonium chloride (12 mg), cooled in an ice-bath, and treated with sodium Z-2-acetamidoethenylthiolate (contanimated by 1 molar equivalent NaCl) (77 mg) in water (25 ml). After stirring vigorously for 25 min. the layers were separated, and the dichloromethane layer was washed with dilute aqueous NaHCO3, followed by brine. After drying (MgSO4) the solution was evaporated in vacuo and the residue was chromatographed on silica gel (230-400 mesh ASTM), eluting with ethyl acetate to give the title compound (118 mg, 52% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04477662
출처 데이터셋uspto-grants-1984_10
ORD IDord-eae508a9ffc14ede9bea75e958bd22a6
출처 메모uspto-grants-1984_10