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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252336Generated: November 3, 2026

p-Toluenesulfonyl isocyanate → HCID 21274226, compound

https://huagongshe.com/reaction/1252336

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonyl isocyanateHCID 77703—
ReactantHCID 13769460HCID 13769460—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTolueneHCID 1140—
ProductHCID 21274226HCID 2127422664.2%

Reaction Steps

A stirred mixture of 0.78 g (0.0021 mole) of 2-[2-chloro-4-fluoro-5-(4-difluoromethyl-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)phenoxy]propionic acid, 0.42 g (0.0021 mole) of p-toluenesulfonyl isocyanate and 0.05 g (0.0004 mole) of 4-dimethylaminopyridine in 50 mL of toluene was heated at reflux for approximately 18 hours. The mixture was allowed to cool to room temperature and was stirred for 24 hours. The solvent was removed by evaporation at reduced pressure to leave a residue. This residue was purified by column chromatography on silica gel, eluting with toluene:ethyl acetate (1:1). The appropriate fractions were combined and evaporated under reduced pressure to yield 0.7 g of N-(4-methylphenylsulfonyl)-2-[2-chloro-4-fluoro-5-(4-difluoromethyl-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)phenoxy]propionamide as a solid, Compound C10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04743291
Source datasetuspto-grants-1988_05
ORD IDord-fafe340e9bf54b19a1d0b6ec510e8566
Source noteuspto-grants-1988_05