Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | 2-Pyrazoline | HCID 66962 | — |
| Edukt | p-(Trifluoromethoxy)phenyl isocyanate | HCID 92298 | — |
| Katalysator | Triethylamine | HCID 8471 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 1-(Phenylcarbamoyl)-2-pyrazoline | HCID 22613946 | — |
Reaktionsschritte
2.76 g (0,008 mol) of 3-(4'-chlorophenyl)-4-(4"-methyl-3"-trifluoromethyl-Δ2" -1",2",4"-triazolin-5"-on-1"-yl)-4,5-dihydropyrazole are dissolved in 20 ml of acetonitrile (anhydrous) at 60° C. until a clear solution has formed, this solution is treated with 1.7 g of 4-trifluoromethoxy-phenyl isocyanate, and 2drops of triethylamine are added. The mixture is subsequently allowed to stand for 2 hours at room temperature. The solvent is subsequently stripped off in vacuo, the residue is treated with 20 ml of diethyl ether and, after 2 hours, the precipitate which has formed is filtered off with suction. 2.0 g (45.6% of theory) of N-(4-trifluormethoxy)-3-(4'-chlorophenyl)-4-(4"-methyl-3"-trifluoromethyl-Δ2" -1",2",4,"-triazolin-5"-on-1"-yl)-4,5-dihydro-1-pyrazole-carboxanilide having a melting point of 241° C. are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05391560 |
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| Quelldatensatz | uspto-grants-1995_02 |
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| ORD ID | ord-d1bc547f902d4e8f83b7be232363093c |
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| Quellennotiz | uspto-grants-1995_02 |
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