Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 4-(Trifluoromethyl)phenyl isocyanate | HCID 73768 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 18980941 | HCID 18980941 | — |
| Reactant | HCID 18981012 | HCID 18981012 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18980932 | HCID 18980932 | — |
Reaction Steps
To 3.5 g (10 mmole) of 2-methanesulfonyloxymethyl-2-propoxy-4'-chloropropiophenone (Example 96e) in 25 ml of methanol was added 1.5 g (18 mmole) of anhydrous sodium acetate, 2.5 g (41 mmole) of acetic acid and 1.0 g (20 mmole) of hydrazine monohydrate. The mixture was refluxed for one hour, concentrated in vacuo, partitioned between diethyl ether and water. The organic layer was washed with dilute aqueous sodium hydroxide and brine and then dried over anhydrous magnesium sulfate, filtered and concentrated to about 25 ml. To this solution of 3-(4-chlorophenyl)-4-methyl-4-propoxy-4,5-dihydro-1H-pyrazole-1-carboxamide was added 2.1 g (11 mmole) of 4-(trifluoromethyl)phenylisocyanate. After stirring for 1 hour the precipitated solid was filtered and washed with diethyl ether and hexanes yielding 3.3 g of the title compound, a white solid, mp 135°-138° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05798311 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-1b21caf811bc4a7ab6f3ce061544b129 |
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| Source note | uspto-grants-1998_08 |
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