Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ici 109,081 | HCID 161928 | — |
| Reactant | 1-Methylcyclopropane-1-carbonyl chloride | HCID 12789939 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20483374 | HCID 20483374 | 65.3% |
Reaction Steps
6.0 g (29.5 millimoles) of 6-(p-aminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone are dissolved in 150 ml of absolute tetrahydrofuran by stirring and heating to 60° C. 4.2 g (35.4 millimoles) of 1-methylcyclopropanecarboxylic acid chloride are added dropwise to the above solution at 60° C., and the reaction mixture is then stirred for 7 hours at the reflux temperature. The product is filtered off at 10° C., washed with water and recrystallized twice from dimethylformamide/water. 5.5 g (65% of theory) of 4,5-dihydro-5-methyl-6-[p-(1-methylcyclopropylcarbonylamino)-phenyl]-3(2H)-pyridazinone are obtained as almost colorless crystals, of melting point 235°-237° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04410529 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-4d27856f29204d2f9c1ed270ef4b1617 |
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| Source note | uspto-grants-1983_10 |
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