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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501241Generated: October 26, 2026

Hydrochloric Acid → N-[5-(5-Trifluoromethyl-[1,3,4]thiadiazol-2-ylsulfamoyl)-indan-2-yl]-acetamide

https://huagongshe.com/reaction/501241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCesium carbonateHCID 10796—
ReactantN-(5-sulfamoyl-2,3-dihydro-1H-inden-2-yl)acetamideHCID 11414131—
Reactant2-Chloro-5-trifluoromethyl-(1,3,4)thiadiazoleHCID 13246789—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-[5-(5-Trifluoromethyl-[1,3,4]thiadiazol-2-ylsulfamoyl)-indan-2-yl]-acetamideHCID 57933510—

Reaction Conditions

Temperature70 °C

Reaction Steps

The mixture of 300 mg of 2-chloro-5-trifluoromethyl-[1,3,4]thiadiazol, 300 mg of N-(5-sulfamoyl-indan-2-yl)-acetamide, 1.8 g cesium carbonate und 10 ml of NMP was stirred at 70° C. for 3 hours. After cooling to room temperature 50 ml of water were added and with 2N hydrochloric acid a pH=3 was adjusted. The product was extracted twice with 30 ml of ethyl acetate, the organic layer was washed with 20 ml of water, dried over sodium sulfate and evaporated in vacuo. The resulting crude material was purified by column chromatography (silica gel, eluent: dichloromethane:methanol=90:10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772257B2
Source datasetuspto-grants-2010_08
ORD IDord-a9680995247b467085d5ffb3416ae18a
Source noteuspto-grants-2010_08