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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1022665Erstellt: 26. Oktober 2026

Water → tert-butyl (6SR,7SR)-7-(3,4-dichlorophenyl)-6-[(methylsulfonyl)amino]-1,4-oxazepane-4-carboxylate

https://huagongshe.com/reaction/1022665

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukttert-butyl (6SR,7SR)-6-amino-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylateHCID 66975299—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-butyl (6SR,7SR)-7-(3,4-dichlorophenyl)-6-[(methylsulfonyl)amino]-1,4-oxazepane-4-carboxylateHCID 6697603382,2%

Reaktionsschritte

Methanesulfonyl chloride (34 mg) was added to a solution of tert-butyl (6SR,7SR)-6-amino-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (90 mg) and triethylamine (33 mg) in THF (5 mL), and the mixture was stirred at room temperature for 1 hr. Water was added to the reaction mixture, 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 (90 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08722662B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-870da08f2e68436e8367b1e693122630
Quellennotizuspto-grants-2014_05