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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400039Generated: October 30, 2026

1,2-Dichloroethane → HCID 49853916, compound

https://huagongshe.com/reaction/1400039

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
Reactant2-Furylglyoxylic acidHCID 73846—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 67515007HCID 67515007—
SolventDimethylformamideHCID 6228—
ProductHCID 49853916HCID 4985391669.6%

Reaction Steps

To a stirred solution of hydrochloride salt of N-{3-[4-(3-aza-bicyclo[3.1.0]hex-1-yl)-phenyl]-2-oxo-oxazolidin-5(S)-yl-methyl}-acetamide (Intermediate IV) (163 mg, 0.46 mmol), in DMF (20 mL), were added α-oxo-2-furanacetic acid (65 mg, 0.46 mmol), EDC (97 mg, 0.51 mmol), HOBt (69 mg, 0.51 mmol) and NMM (0.11 mL, 1.02 mmol) at 0° C. The reaction mixture was stirred at r.t. and progress of the reaction was monitored by TLC. On completion, DMF was evaporated in vacuo and residue was dissolved in chloroform (50 mL). The organic layer was washed with water (25 mL), brine (25 mL), dried over anhydrous sodium sulphate and concentrated in vacuo. The residue was purified by column chromatography (silica gel, 0.4:9.6 MeOH:CHCl3) to provide the title compound (140 mg, 69%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906913B2
Source datasetuspto-grants-2014_12
ORD IDord-464ef2908c5d4e37868b47d06c669103
Source noteuspto-grants-2014_12