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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 526948생성일: 2026년 10월 26일

Methyl chloroformate → Methyl N-[(1R,3S)-3-benzyloxycarbonylaminocyclohexyl]carbamate

https://huagongshe.com/reaction/526948

반응식

참여 물질

역할이름HCID투입량
반응물Methyl chloroformateHCID 6586—
반응물TriethylamineHCID 8471—
반응물Benzyl ((1S,3R)-3-aminocyclohexyl)carbamateHCID 69756715—
용매TetrahydrofuranHCID 8028—
생성물Methyl N-[(1R,3S)-3-benzyloxycarbonylaminocyclohexyl]carbamateHCID 68007620—

반응 단계

Benzyl N-[(1S,3R)-3-aminocyclohexyl]carbamate, 18e, (0.99 g, 3.99 mmol) was dissolved in THF (20 mL) and treated with methyl chloroformate (0.62 mL, 7.97 mmol), followed by triethylamine (1.67 mL, 11.96 mmol). After stirring for 1 hour at room temperature, the solvent was evaporated under reduced pressure and the residue was diluted into 1:3 mixture of CH2Cl2:EtOAc (130 mL) and washed with 1N HCl (50 mL) and 2N Na2CO3 (50 mL). The organic layer was dried over Na2SO4 and concentrated under reduced pressure to afford the desired product, 19a, as a white solid (1.09 g, 89% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09345708B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-55bcb3c49562482bb9f7303c3618d05e
출처 메모uspto-grants-2016_05