Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dimethylazanium;chloride | HCID 12954980 | — |
| Reactant | HCID 14623682 | HCID 14623682 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 14623684 | HCID 14623684 | — |
Reaction Steps
In a similar manner to Example 3b) a mixture of 6-(4-propionylphenyl)pyridazin-3(2H)-one (2.28 g), formaldehyde (37% solution, 1 ml) and dimethylammonium chloride (1.25 g) in acetic anhydride (8 ml) was stirred at 90° C. for 11/2 hours. The cooled solution was poured into dry acetone (150 ml) and was evaporated to dryness under reduced pressure to afford a yellow oil. Trituration with dry acetone afforded 6-[4-(3-dimethylamino-2-methylpropionyl)phenyl]pyridazin-3(2H)-one hydrochloride (2.12 g), as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04904664 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-aa5e2c1cc4774dcbb679cc56fd99f18d |
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| Source note | uspto-grants-1990_02 |
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