Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940621Generated: October 30, 2026

Dimethyl Sulfoxide → N-[2-(4,5,7-trifluorobenzothiazol-2-ylthio)acetyl]-N-phenylglycine

https://huagongshe.com/reaction/1940621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantBromoacetic AcidHCID 6227—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4,5,7-trifluorobenzothiazol-2-ylthio)-N-phenylacetamideHCID 21463540—
SolventWaterHCID 962—
ProductN-[2-(4,5,7-trifluorobenzothiazol-2-ylthio)acetyl]-N-phenylglycineHCID 2146353419.4%

Reaction Steps

To DMSO (5 ml) was added 2-(4,5,7-trifluorobenzothiazol-2-ylthio)-N-phenylacetamide (354 mg, 1 mmol), bromoacetic acid (278 mg, 2 mmol) and potassium carbonate (414 mg, 3 mmol) and the mixture was stirred at room temperature for 5 hours under a nitrogen stream. The resultant reaction mixture was diluted with water and washed with ethyl acetate. The aqueous phase was acidified with 7% hydrochloric acid and extracted with ethyl acetate. The organic phase was washed with water, dried and then evaporated to yield crude crystals, which were recrystallized from ethyl acetate-hexane to give N-[2-(4,5,7-trifluorobenzothiazol-2-ylthio)acetyl]-N-phenylglycine (80 mg, 19%) as slightly yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05700819
Source datasetuspto-grants-1997_12
ORD IDord-642d5fff46b94ead8fb595727f386a5f
Source noteuspto-grants-1997_12