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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437700Generated: October 26, 2026

Dibenzo-18-crown-6 → N'-acetyl-N'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylurea

https://huagongshe.com/reaction/437700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzo-18-crown-6HCID 26541—
ReactantPotassium AcetateHCID 517044—
ReactantN'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylchloroformamidineHCID 53844528—
SolventAcetonitrileHCID 6342—
ProductN'-acetyl-N'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylureaHCID 21426738—

Reaction Steps

A mixture of 4.9 g of potassium acetate, and a catalytic amount of 2,3,11,12-dibenzo-1,4,7,10,13,16-hexaoxacyclooctadeca-2,11-diene in 60 ml of acetonitrile was stirred vigorously during 45 minutes. Then 12.8 grams of N'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylchloroformamidine in acetonitrile were added. The reaction mixture stood at ambient temperature for 16 hours. Thin layer chromatographic analysis indicated that the reaction had not gone to completion. The reaction mixture was stirred at ambient temperature for 3 days, at which time thin layer chromatographic analysis indicated the reaction to be complete. The reaction mixture was filtered and the filtrate evaporated, under reduced pressure. The residue was slurried in diethyl ether to give a solid. The solid was collected by filtration, then slurried in water to give 10.8 g of N'-acetyl-N'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylurea; mp 128°-130°. The nmr and the ir spectra were consistent with the assigned structure. The uv spectrum confirmed the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04032321
Source datasetuspto-grants-1977_06
ORD IDord-59d5579531674959acbb64fc65e91049
Source noteuspto-grants-1977_06