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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41746생성일: 2026년 10월 23일

Heptanol → [(1R)-1-({[(2,3-difluorobenzoyl)amino]acetyl}amino)-3-methylbutyl]boronic acid

https://huagongshe.com/ko/reaction/41746

반응식

참여 물질

역할이름HCID투입량
반응물HeptanolHCID 8129—
반응물2,3-difluoro-N-[2-({(1R)-3-methyl-1-[(3aR,4R,6R,7aS)-3a,5,5-trimethylhexahydro-4,6-methano-1,3,2-benzodioxaborol-2-yl]butyl} amino)-2-oxoethyl]benzamideHCID 67369041—
반응물HCID 178450000HCID 178450000—
용매MethanolHCID 887—
생성물[(1R)-1-({[(2,3-difluorobenzoyl)amino]acetyl}amino)-3-methylbutyl]boronic acidHCID 25022369—

반응 단계

To a solution of 2,3-difluoro-N-[2-({(1R)-3-methyl-1-[(3aR,4R,6R,7aS)-3a,5,5-trimethylhexahydro-4,6-methano-1,3,2-benzodioxaborol-2-yl]butyl}amino)-2-oxoethyl]benzamide (0.536 g, 1.2 mmol) in methanol/1N HCl (1:1) (1.5 mL) were added heptanol (1 mL) and isobutyl boronate (0.207 g, 2.0 mmol). The reaction mixture was allowed to stir overnight. The heptanol layer was separated and the methanol/HCl layer was concentrated. The crude product was purified by reverse phase HPLC to give [(1R)-1-({[(2,3-difluorobenzoyl)amino]acetyl}amino)-3-methylbutyl]boronic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530694B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-d7af6213e11c4fe4abfafafb130efe8d
출처 메모uspto-grants-2013_09