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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979278Generated: October 31, 2026

2-Chloroethyl methyl ether → N-[[(5S)-3-[3-fluoro-4-(2-methoxyethylsulfanyl)phenyl]-2-oxo-oxazolidin-5-yl]methyl]acetamide

https://huagongshe.com/reaction/1979278

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroethyl methyl etherHCID 12316—
Reactant5-(S)-Acetamidomethyl-3-[4'-triphenylmethylthio-3'-fluorophenyl]oxazolidine-2-oneHCID 22966197—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-[[(5S)-3-[3-fluoro-4-(2-methoxyethylsulfanyl)phenyl]-2-oxo-oxazolidin-5-yl]methyl]acetamideHCID 485759—

Reaction Steps

Prepared according to Method B of the General Procedures for Preparation of 5-(S)-(N-Acylaminomethyl)-3-[4′-(substituted)thio-3′-fluorophenyl]oxazoli-dine-2-ones from 5-(S)-acetamidomethyl-3-[4′-(triphenylmethyl)thio-3′-fluorophenyl]oxazolidine-2-one with 2-chloroethyl methyl ether (0.036 g, 0.38 mmol) in N-methylpyrrolidine-2-one (1 mL). The synthesis was performed at r.t. for 2 h. The crude product was purified by TLC (eluent: 10% methanol in dichloromethane). Yield 0.034 g (52%). MS (m/z): 343 [M+H]+. 1H NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239152B1
Source datasetuspto-grants-2001_05
ORD IDord-ff6a05813f3f47be87935f4d9f94502f
Source noteuspto-grants-2001_05