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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1022626생성일: 2026년 10월 27일

Triethylamine → tert-butyl (6R,7R)-7-(4-chloro-3-fluorophenyl)-6-{[(methoxyacetyl)amino]methyl}-1,4-oxazepane-4-carboxylate

https://huagongshe.com/reaction/1022626

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methoxyacetyl chlorideHCID 96623—
반응물tert-butyl (6R,7R)-6-(aminomethyl)-7-(4-chloro-3-fluorophenyl)-1,4-oxazepane-4-carboxylateHCID 66975002—
용매TetrahydrofuranHCID 8028—
생성물tert-butyl (6R,7R)-7-(4-chloro-3-fluorophenyl)-6-{[(methoxyacetyl)amino]methyl}-1,4-oxazepane-4-carboxylateHCID 6697528371.1%

반응 단계

To a solution of tert-butyl (6R,7R)-6-(aminomethyl)-7-(4-chloro-3-fluorophenyl)-1,4-oxazepane-4-carboxylate (1.30 g) in THF (18 mL) were added triethylamine (0.757 ml) and methoxyacetyl chloride (472 mg), and the mixture was stirred at room temperature for 4 hr. To the reaction mixture was added distilled water, and the mixture was extracted with ethyl acetate. The diluted solution was washed with distilled water and brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (hexane/ethyl acetate) to give the title compound (1.11 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722662B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-da2c08cff5884fc2898eb18c58cfd536
출처 메모uspto-grants-2014_05