Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434682Generated: October 30, 2026

Dimethylformamide → 4-cyano-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide

https://huagongshe.com/reaction/1434682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Acetyl-n-(thiazol-2-yl)benzenesulfonamideHCID 21082529—
SolventWaterHCID 962—
Product4-cyano-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamideHCID 67001447—

Reaction Steps

To a suspension of 4-acetyl-N-thiazol-2-yl-benzenesulfonamide (10 mmol) and potassium carbonate (15 mmol) in DMF (30 mL) was added chloro-methoxy-methane (10 mmol) and the mixture was stirred for 4 h. The reaction mixture was diluted with water (30 mL) and the resulting mixture was extracted with ethyl acetate. The organic phase was washed with brine, dried over MgSO4, and concentrated in vacuo. The crude product was purified by column chromatography to give 4-cyano-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide (5.2 mmol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615569B2
Source datasetuspto-grants-2009_11
ORD IDord-05c3d9da90e94aa78be6e3ff3ca93dd7
Source noteuspto-grants-2009_11