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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022761Generated: November 1, 2026

Water → tert-butyl (6R,7R)-6-[(3-carbamothioyl-2-oxopyridin-1(2H)-yl)methyl]-7-(4-chloro-3-fluorophenyl)-1,4-oxazepane-4-carboxylate

https://huagongshe.com/reaction/1022761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantDiethyldithiophosphateHCID 53249491—
ReactantHCID 66976171HCID 66976171—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
SolventHydrogen chloride-ethyl acetateHCID 21866389—
Producttert-butyl (6R,7R)-6-[(3-carbamothioyl-2-oxopyridin-1(2H)-yl)methyl]-7-(4-chloro-3-fluorophenyl)-1,4-oxazepane-4-carboxylateHCID 8666387360.2%

Reaction Steps

Diethyl dithiophosphate (0.189 mL, 1.13 mmol) was added to a solution (5 mL, 20.00 mmol) of tert-butyl (6R,7R)-7-(4-chloro-3-fluorophenyl)-6-[(3-cyano-2-oxopyridin-1(2H)-yl)methyl]-1,4-oxazepane-4-carboxylate (348 mg, 0.75 mmol) in 4 N hydrogen chloride-ethyl acetate. The reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure. The residue was diluted with saturated aqueous sodium hydrogen carbonate solution (10 mL) and ethyl acetate (10 ml), and di-tert-butyl dicarbonate (0.210 mL, 0.90 mmol) was added. The reaction mixture was stirred at room temperature for 4 hr. To the reaction mixture was added water, 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 (225 mg, 0.454 mmol, 60.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722662B2
Source datasetuspto-grants-2014_05
ORD IDord-73cf7a0125834b86b2008b92e8493dba
Source noteuspto-grants-2014_05