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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231141Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 178431394, compound

https://huagongshe.com/reaction/231141

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 178522558HCID 178522558—
SolventAcetoneHCID 180—
ProductHCID 178431394HCID 178431394156.8%

Reaction Conditions

Temperature20 °C

Reaction Steps

A suspension of 3 g of the product of Example 2 in 80 ml of acetone was heated to reflux and 0.3 g of p-toluene sulfonic acid were added. The mixture was refluxed for 5 hours, was cooled to 20° C. and was vacuum filtered. The crystals were dried under reduced pressure and dissolved in 100 ml of tetrahydrofuran warmed to 40° C. The mixture was filtered and was concentrated to one half volume. The mixture was cooled to 20° C. and ether was added. The mixture was vacuum filtered and the crystals were washed with ether and dried to obtain 1.2 g of 2-(2,2-dimethyl-1,3-dioxolan-4-yl)-4-hydroxy-N-(2-thiazolyl)-8-trifluoromethyl-3-quinoline-carboxamide melting at 250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845105
Source datasetuspto-grants-1989_07
ORD IDord-028d6fdd498e4e4b932db908429a542d
Source noteuspto-grants-1989_07