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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1852118생성일: 2026년 10월 27일

Methanol → (2S,4R)-1-((2S,3R)-2-((tert-butoxycarbonyl)amino)-3,5-dimethylnon-8-enoyl)-4-hydroxypyrrolidine-2-carboxylic acid

https://huagongshe.com/reaction/1852118

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Lithium HydroxideHCID 3939—
반응물(2S,4R)-methyl 1-((2S,3R)-2-((tert-butoxycarbonyl)amino)-3,5-dimethylnon-8-enoyl)-4-hydroxypyrrolidine-2-carboxylateHCID 86683197—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(2S,4R)-1-((2S,3R)-2-((tert-butoxycarbonyl)amino)-3,5-dimethylnon-8-enoyl)-4-hydroxypyrrolidine-2-carboxylic acidHCID 86683196115%

반응 단계

(2S,4R)-methyl 1-((2S,3R)-2-((tert-butoxycarbonyl)amino)-3,5-dimethylnon-8-enoyl)-4-hydroxypyrrolidine-2-carboxylate (10.8 g, 25.3 mmol) was dissolved in THF (50 mL), MeOH (50 mL) and to this solution was added LiOH (2.425 g, 101 mmol) in Water (50.0 mL). The reaction mixture was stirred at rt for 16 h. The solvent was removed under vacuum and the resulting aqueous residue was diluted with water, and EtOAc. The mixture was neutralised with 1 N HCl and adjusted the pH ˜2.5 and the mixture was extracted with EtOAc. The organic layer was collected, washed with brine, dried over Na2SO4, and concentrated to give (2S,4R)-1-((2S,3R)-2-((tert-butoxycarbonyl)amino)-3,5-dimethylnon-8-enoyl)-4-hydroxypyrrolidine-2-carboxylic acid (12 g, 29.1 mmol, 115% yield) as yellow viscous oil. MS: MS m/z 413.2 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08957203B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-078c31a7b5d6441486a4a9d39565d6b9
출처 메모uspto-grants-2015_02