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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133129Generated: October 23, 2026

1,2-Dichloroethane → tert-Butyl [(3R,6S)-6-(2,3-difluorophenyl)-2-oxoazepan-3-yl]carbamate

https://huagongshe.com/en/reaction/133129

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
ReactantHOAtHCID 181649—
ReactantSodium BicarbonateHCID 516892—
Reactant(5S)-N2,N2-Bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-D-lysineHCID 67526479—
SolventDichloromethaneHCID 6344—
Producttert-Butyl [(3R,6S)-6-(2,3-difluorophenyl)-2-oxoazepan-3-yl]carbamateHCID 23657400—

Reaction Steps

To a solution (5S)—N2,N2-bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-D-lysine from Step D (22.0 g, 48.0 mmol) in CH2Cl2 (700 mL) were added EDC (11.0 g, 57.6 mmol) and HOAT (3.27 g, 24.0 mmol) followed by triethylamine (10.0 mL, 72.0 mmol). After 1 h, aqueous NaHCO3 was added, the layers were separated, and the aqueous phase was extracted with CH2Cl2. The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography, eluting with CH2Cl2:MeOH—90:10, to give the title compound. MS: m/z=341 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390798B2
Source datasetuspto-grants-2008_06
ORD IDord-558f8849205643dfa6130d05bee5202e
Source noteuspto-grants-2008_06