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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164408Generated: October 31, 2026

Methoxycarbonyl isothiocyanate → 1-[2-(3-Acetylureido)-5-phenoxysulfonylphenyl]-3-methoxycarbonylthiourea

https://huagongshe.com/reaction/2164408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxycarbonyl isothiocyanateHCID 552246—
Reactant2-(3-Acetylureido)-5-phenoxysulfonylanilineHCID 15585384—
Solvent1,4-DioxaneHCID 31275—
Product1-[2-(3-Acetylureido)-5-phenoxysulfonylphenyl]-3-methoxycarbonylthioureaHCID 15585385—

Reaction Steps

17.5 g of 2-(3-acetylureido)-5-phenoxysulfonylaniline and 15 ml of methoxycarbonyl isothiocyanate in 150 ml of dioxane are heated at 80° C. for 5 minutes, and then stirring is continued without heating. After slowly cooling down to room temperature, the dioxane is distilled out under reduced pressure. The residue is dissolved in dimethylformamide, the solution is treated with active charcoal and evaporated and then methanol is added. After cooling down, the precipitate is filtered off with suction and washed with methanol and diisopropyl ether. Melting point 215° C., decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04504490
Source datasetuspto-grants-1985_03
ORD IDord-c789a8dbaaaa4effbd53aff75238dd3a
Source noteuspto-grants-1985_03