HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Benzyl-4,5-dichloro-2,3-dihydropyridazin-3-one → 2-Benzyl-4-chloro-5-methoxypyridazin-3(2h)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Benzyl-4,5-dichloro-2,3-dihydropyridazin-3-one | HCID 722438 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Benzyl-4-chloro-5-methoxypyridazin-3(2h)-one | HCID 737015 | — |
Reaction Steps
To a solution of 2-benzyl-4,5-dichloro-2H-pyridazine-3-one (22.31 g, 87.47 mmol), prepared as described in Example 244A, in dry MeOH (175 mL) at 0° C., was added dropwise a solution of sodium methoxide in methanol (25% weight in MeOH, 25 mL). The mixture was slowly warmed up to room temperature and stirred for 18 h. The reaction mixture was diluted with methylene chloride (200 mL) and filtered. The filtrate was concentrated to afford the title compound, 2-benzyl-4-chloro-5-methoxypyridazin-3(2H)-one (22.2 g) which was >95% pure as judged by HPLC and was used in the next reaction, Example 354B, without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07378418B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-dc4920055d6943cfbcf8e8ea451d75fe |
| Source note | uspto-grants-2008_05 |