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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2038564생성일: 2026년 10월 26일

Methanol → (5S,8S)-3-(3-chlorophenyl)-7-((S)-2-(cyclopentyloxycarbonylamino)-3,3-dimethylbutanoyl)-2-oxo-1-oxa-3,7-diazaspiro[4.4]nonane-8-carboxylic acid

https://huagongshe.com/reaction/2038564

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Lithium HydroxideHCID 3939—
반응물(5S,8S)-methyl-3-(3-chlorophenyl)-7-((S)-2-(cyclopentyloxycarbonylamino)-3,3-dimethylbutanoyl)-2-oxo-1-oxa-3,7-diazaspiro[4.4]nonane-8-carboxylateHCID 59547346—
용매TetrahydrofuranHCID 8028—
생성물(5S,8S)-3-(3-chlorophenyl)-7-((S)-2-(cyclopentyloxycarbonylamino)-3,3-dimethylbutanoyl)-2-oxo-1-oxa-3,7-diazaspiro[4.4]nonane-8-carboxylic acidHCID 5954731846.3%

반응 단계

(5S,8S)-methyl-3-(3-chlorophenyl)-7-((S)-2-(cyclopentyloxycarbonylamino)-3,3-dimethylbutanoyl)-2-oxo-1-oxa-3,7-diazaspiro[4.4]nonane-8-carboxylate (C3) (22 mg, 41 μmol, 1 eq.) was diluted with dry THF (0.5 mL) then 1 M LiOH (82 μL, 82 μmol, 2 eq.) and MeOH (20 μL) was added. The reaction was stirred overnight at room temp. and concentrated to give 10 mg (19 μmol) of (5S,8S)-3-(3-chlorophenyl)-7-((S)-2-(cyclopentyloxycarbonylamino)-3,3-dimethylbutanoyl)-2-oxo-1-oxa-3,7-diazaspiro[4.4]nonane-8-carboxylic acid (D3). LC MS+: 522.35 at 3.14 min (10-90%, 3-5 min, Formic Acid).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08575208B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-59d921abbb714fa48c34ebcddc60dcf4
출처 메모uspto-grants-2013_11