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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501111생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/501111

반응식

참여 물질

역할이름HCID투입량
반응물L-MethionineHCID 6137—
반응물Benzyl (3R)-1-(2,4-dimethoxybenzyl)-2-oxo-6-phenyl-2,3,4,7-tetrahydro-1H-azepin-3-ylcarbamateHCID 60037872—
용매DichloromethaneHCID 6344—
용매Trifluoroacetic acidHCID 6422—
생성물Benzyl (3R)-2-oxo-6-phenyl-2,3,4,7-tetrahydro-1H-azepin-3-ylcarbamateHCID 6003784676%

반응 단계

A solution of L-methionine (2.56 g, 17.2 mmol) in trifluoroacetic acid (15 mL) was added to a solution of benzyl (3R)-1-(2,4-dimethoxybenzyl)-2-oxo-6-phenyl-2,3,4,7-tetrahydro-1H-azepin-3-ylcarbamate (0.84 g, 1.72 mmol) in dichloromethane (20 mL). After 18 h, the mixture was concentrated and water was added. The mixture was extracted with ethyl acetate, washed with water (2×), saturated aqueous sodium bicarbonate (2×), saturated brine, dried over magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (5% ethyl acetate/hexanes →50% ethyl acetate/hexanes) gave the title compound (0.44 g). MS 337 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772224B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-53bcf3dae52640919fb4b7a16a649e05
출처 메모uspto-grants-2010_08