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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1022628생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1022628

반응식

참여 물질

역할이름HCID투입량
반응물Ethoxyacetic acidHCID 12301—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물tert-butyl (6R,7R)-6-(aminomethyl)-7-(4-chloro-3-fluorophenyl)-1,4-oxazepane-4-carboxylateHCID 66975002—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물tert-butyl (6R,7R)-7-(4-chloro-3-fluorophenyl)-6-{[(ethoxyacetyl)amino]methyl}-1,4-oxazepane-4-carboxylateHCID 6697526283.6%

반응 단계

To a solution of tert-butyl (6R,7R)-6-(aminomethyl)-7-(4-chloro-3-fluorophenyl)-1,4-oxazepane-4-carboxylate (150 mg), ethoxyacetic acid (35 mg), 1H-benzotriazol-1-ol (67.8 mg) and triethylamine (0.146 ml) in THF (2.1 mL) was added N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (96 mg), and the mixture was stirred overnight. To the reaction mixture was added distilled water, and the mixture was extracted with ethyl acetate. The extract was washed with distilled water and brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (hexane/ethyl acetate) to give the title compound (125 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722662B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-eac980e094d04dc183f4ad69722e3411
출처 메모uspto-grants-2014_05