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HRID 1409862作成日:2026年10月26日

Acetic Acid → HCID 178474964、化合物

https://huagongshe.com/reaction/1409862

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Sodium HydroxideHCID 14798—
反応物DiisopropylethylamineHCID 81531—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物HCID 178478713HCID 178478713—
溶媒DimethylformamideHCID 6228—
生成物HCID 178474964HCID 17847496442.3%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08921397B2
出典データセットuspto-grants-2014_12
ORD IDord-3e1adfceaa8546648dde077ee7627d89
出典メモuspto-grants-2014_12