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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dibenzo-18-crown-6 | HCID 26541 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | N'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylchloroformamidine | HCID 53844528 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N'-acetyl-N'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylurea | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04032321 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-59d5579531674959acbb64fc65e91049 |
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| Source note | uspto-grants-1977_06 |
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