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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723795Generated: October 30, 2026

1-Chloroethyl chloroformate → HCID 69363543, compound

https://huagongshe.com/reaction/723795

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 69364497HCID 69364497—
CatalystDiisopropylethylamineHCID 81531—
SolventDichloromethaneHCID 6344—
ProductHCID 69363543HCID 6936354386.7%

Reaction Steps

1-Chloroethyl chloroformate (1.18 g, 8.3 mM) was added dropwise, under an atmosphere of nitrogen, to a stirred solution of (5R)-3-(4-(1-benzyl-1,2,5,6-tetrahydropyridin-4-yl)-3-fluoro-phenyl)-5-(tetrazol-2-ylmethyl)oxazolidin-2-one (2.56 g, 5.90 mM) and N,N-diisopropylethylamine (0.230 mg, 1.77 mM) in dichloromethane (50 ml) with cooling in ice/water. The reaction was stirred for 30 minutes at ice temperature, and the brown solution purified by MPLC on silica, eluting with 75% ethyl acetate in isohexane. The resulting carbamate intermediate was dissolved in methanol (60 ml) and heated at 60° for 30 minutes. Evaporation of the solvent and trituration with diethyl ether gave the title compound (1.76 g) as its hydrochloride salt. MS (ESP): 345 (MH+) for C16H17FN6O2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141583B2
Source datasetuspto-grants-2006_11
ORD IDord-7a33acd654d04ddbb063a5d030dfee22
Source noteuspto-grants-2006_11