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HRID 41746作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物HeptanolHCID 8129—
反応物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]benzamideHCID 67369041—
反応物HCID 178450000HCID 178450000—
溶媒MethanolHCID 887—
生成物[(1R)-1-({[(2,3-difluorobenzoyl)amino]acetyl}amino)-3-methylbutyl]boronic acidHCID 25022369—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530694B2
出典データセットuspto-grants-2013_09
ORD IDord-d7af6213e11c4fe4abfafafb130efe8d
出典メモuspto-grants-2013_09