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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828827Generated: November 1, 2026

p-Toluenesulfonyl isocyanate → HCID 22058622, compound

https://huagongshe.com/reaction/1828827

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonyl isocyanateHCID 77703—
ReactantHCID 22058647HCID 22058647—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22058622HCID 2205862275.6%

Reaction Steps

4-Chloro-1-(2-chloro-4-(1-pentyloxy)benzyl)-5-hydroxymethyl-2-methyl-1H-imidazole (150 mg) was dissolved in 1,4-dioxane (1.5 ml) and p-toluenesulfonyl isocyanate (99 mg) was added at room temperature. The reaction mixture was stirred at room temperature for 1 hr and concentrated under reduced pressure. To the residue was added ethanol (5 ml) and the precipitated crystals were collected by filtration. The crystals were dissolved in ethyl acetate (2 ml), and hexane (13 ml) was added on an oil bath at 70° C. The mixture was allowed to cool and the precipitated crystals were collected by filtration. The crystals were dried by heating under reduced pressure to give (4-chloro-1-(2-chloro-4-(1-pentyloxy)benzyl)-2-methyl-1H-imidazol-5-yl)methyl N-(4-methylbenzenesulfonyl)carbamate (176 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060721B1
Source datasetuspto-grants-2006_06
ORD IDord-1c0a7e62692e409cb80118b054fb085e
Source noteuspto-grants-2006_06