Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 6-(4-Methoxyphenyl)-4,5-dihydropyridazin-3(2H)-one | HCID 689109 | — |
| Reactant | Potassium hydroxide ethanol | HCID 21946426 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12391761 | HCID 12391761 | 76% |
Reaction Steps
6-(4-methoxy-phenyl)-4,5-dihydro-2H-pyridazin-3-one (1.65 g, 7.5 mmol) in 15 mL of EtOH was heated to 80° C. as 20 mL of 4% of KOH/EtOH solution was added dropwise. After 5 min., benzaldehyde (1.0 eq. 0.76 mL) was added and the mixture stirred at 80° C. for 2 h. The reaction was cooled to rt., poured into ice-H2O (75 mL) and the resulting solid was collected and crystallized from EtOH to give 1.67 g (76%) of intermediate 4-benzyl-6-(4-methoxy-phenyl)-2H-pyridazin-3-one: MS m/z 293 (M+H). This intermediate was used to prepare examples 45 and example 46.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586588B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-c14a3cffcd3442c4a3deb0bbcf242167 |
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| Source note | uspto-grants-2013_11 |
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