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HRID 493630생성일: 2026년 10월 25일

Iodine → (3R,6S)-3-Amino-1-(2-methoxyethyl)-6-phenylazepan-2-one

https://huagongshe.com/reaction/493630

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Diethyl EtherHCID 3283—
반응물1-Bromo-2,3-dichlorobenzeneHCID 42066—
반응물MagnesiumHCID 5462224—
반응물benzyl (2R,5E)-2-[bis(tert-butoxycarbonyl)amino]-6-nitrohex-5-enoateHCID 25034374—
생성물(3R,6S)-3-Amino-1-(2-methoxyethyl)-6-phenylazepan-2-oneHCID 60037849—

반응 단계

To a slurry of 1-bromo-2,3-dichlorobenzene (1.46 g, 6.46 mmol) in diethyl ether (10 mL) was added magnesium (0.157 g, 6.46 mmol) and a crystal of iodine. This mixture was refluxed for 3 h, and then cooled to room temperature. A solution of benzyl (2R,5E)-2-[bis(tert-butoxycarbonyl)amino]-6-nitrohex-5-enoate (0.50 g, 1.08 mmol) in diethyl ether (10 mL) was cooled to 0° C., and 2.0 mL of the Grignard solution prepared above was added. After 1 and 2 h, respectively, 2.0 and 1.0 mL of the Grignard solution was added. The reaction was quenched with a saturated aqueous solution of ammonium chloride, the phases separated and the organic phase washed with saturated aqueous sodium potassium tartrate and brine. The combined organics were dried over magnesium sulfate, filtered and concentrated to give a residue that was purified by silica gel chromatography (0%→3% methanol/dichloromethane) to give the title compound (0.52 g). MS 411.0 (M+1-2Boc).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534784B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-5edab4b4a3e1405bb742569144dfedc5
출처 메모uspto-grants-2009_05