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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20117생성일: 2026년 10월 23일

L-Methionine → Benzyl (3R)-6-bromo-2-oxo-2,3,4,7-tetrahydro-1H-azepin-3-ylcarbamate

https://huagongshe.com/ko/reaction/20117

반응식

참여 물질

역할이름HCID투입량
반응물L-MethionineHCID 6137—
반응물Benzyl (3R)-6-bromo-1-(2,4-dimethoxybenzyl)-2-oxo-2,3,4,7-tetrahydro-1H-azepin-3-ylcarbamateHCID 60037867—
용매DichloromethaneHCID 6344—
용매Trifluoroacetic acidHCID 6422—
생성물Benzyl (3R)-6-bromo-2-oxo-2,3,4,7-tetrahydro-1H-azepin-3-ylcarbamateHCID 2365709127.2%

반응 단계

A solution of L-methionine (274 mg, 1.84 mmol) in trifluoroacetic acid (5 mL) was added to a solution of benzyl (3R)-6-bromo-1-(2,4-dimethoxybenzyl)-2-oxo-2,3,4,7-tetrahydro-1H-azepin-3-ylcarbamate (90 mg, 0.184 mmol) in dichloromethane (5 mL). After 18 h, the mixture was concentrated. Purification by reverse phase HPLC (C-18, 95% water/acetonitrile→5% water/acetonitrile with 0.1% trifluoroacetic acid) gave the title compound (17 mg). MS 339 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745427B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-9f6e6e77a9204b188026d604d11c70f4
출처 메모uspto-grants-2010_06