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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1022663Erstellt: 26. Oktober 2026

Acetic Acid → tert-butyl (6SR,7SR)-6-amino-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate

https://huagongshe.com/reaction/1022663

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt2,2'-BipyridineHCID 1474—
EduktSodium borohydrideHCID 4311764—
Edukttert-butyl (6SR,7SR)-6-azido-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylateHCID 86663863—
KatalysatorCobalt dibromideHCID 24610—
LösungsmittelEthanolHCID 702—
Produkttert-butyl (6SR,7SR)-6-amino-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylateHCID 6697529975,8%

Reaktionsbedingungen

Temperatur2.5 °C

Reaktionsschritte

To a solution of cobalt bromide (15 mg) in ethanol (5 mL) was added 2,2′-bipyridyl (33 mg), sodium tetrahydroborate (53 mg) was added, and the mixture was stirred at 0-5° C. for 5 min. To the reaction mixture was added a solution of tert-butyl (6SR,7SR)-6-azido-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (270 mg) in ethanol (5 mL), and the mixture was stirred at 0-5° C. for 30 min. Acetic acid was added to the reaction mixture, and the mixture was stirred at room temperature for 5 min. The solvent was evaporated under reduced pressure. The residue was neutralized with saturated aqueous sodium hydrogen carbonate, and the mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (191 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08722662B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-1253be1d357643009d53a3f1f5bbcd89
Quellennotizuspto-grants-2014_05