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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41746Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHeptanolHCID 8129—
Edukt2,3-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—
EduktHCID 178450000HCID 178450000—
LösungsmittelMethanolHCID 887—
Produkt[(1R)-1-({[(2,3-difluorobenzoyl)amino]acetyl}amino)-3-methylbutyl]boronic acidHCID 25022369—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530694B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-d7af6213e11c4fe4abfafafb130efe8d
Quellennotizuspto-grants-2013_09