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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1409862생성일: 2026년 10월 25일

Acetic Acid → HCID 178474964, 화합물

https://huagongshe.com/reaction/1409862

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium HydroxideHCID 14798—
반응물DiisopropylethylamineHCID 81531—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물HCID 178478713HCID 178478713—
용매DimethylformamideHCID 6228—
생성물HCID 178474964HCID 17847496442.3%

반응 단계

To a stirred mixture of trans-4-[2-(4-benzofuran-3-yl-piperidin-1-yl)-ethyl]-cyclohexylamine dihydrochloride (intermediate A) (100 mg, 0.25 mmol) in DMF (3 ml) was added N,N-diisopropylethylamine (113 mg, 150 μl, 0.88 mmol), acetic acid (22.6 mg, 21.5 μl, 376 μmol) and TBTU (121 mg, 376 μmol). The mixture was allowed to stir at room temperature for 16 h, poured into ice/water (5 ml) and 1N NaOH (5 ml) and extracted with dichloromethane (2×20 ml). The combined organic layers were washed with brine (10 ml), dried (MgSO4) and evaporated. The crude material was further purified by flash chromatography on silica gel (dichloromethane/MeOH/NH4OH 150:10:1) and trituration from dichloromethane (1 ml) and heptane (5 ml) for 30 min. The precipitate was collected by filtration, washed with heptane and dried to yield the title compound as a white solid (39 mg, 42%), MS (ISP) m/z=369.3 [(M+H)+], mp 162° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921397B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-3e1adfceaa8546648dde077ee7627d89
출처 메모uspto-grants-2014_12