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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531381Generated: November 1, 2026

1,2-Dichloroethane → HCID 76674797, compound

https://huagongshe.com/reaction/531381

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant2-OxazolidinoneHCID 73949—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-CyclopropylmethanesulfonamideHCID 22149151—
ReactantHCID 66870865HCID 66870865—
SolventDichloromethaneHCID 6344—
ProductHCID 76674797HCID 7667479744.2%

Reaction Steps

To acid 138 (212 mg, 0.276 mmol) dissolved in dichloromethane (7 mL) was added EDC (69 mg, 0.359 mmol) and the reaction mixture was stirred at room temperature. After 7 hours TLC and LC-MS indicated complete conversion of the starting material into the corresponding oxazolidinone. The reaction mixture was diluted with dichloromethane (20 mL) and the organic phase was washed twice with water after which the organic phase was dried, filtered, and concentrated. The residue was dissolved in dichloromethane (5 mL) and cyclopropylmethyl sulfonamide (53 mg, 0.394 mmol) and DBU (78 μL, 0.525 mmol) were added and the reaction mixture was stirred at room temperature for 20 hours. The mixture was diluted with dichloromethane (30 mL) and the organic phase was washed twice with 10% citric acid and once with brine. The organic phase was dried, filtered and concentrated and the crude product was purified by flash column chromatography (toluene/ethyl acetate 1:1, 1:2, ethyl acetate, ethyl acetate/methanol 9:1) to give the title compound (108 mg, 44%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353103B2
Source datasetuspto-grants-2016_05
ORD IDord-11ca258f7b5842039395705035f5270e
Source noteuspto-grants-2016_05