HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Methyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Chloro-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylic acid | HCID 66674132 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylate | HCID 57886211 | 17% |
Reaction Steps
A solution of 4-chloro-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylic acid (390 mg, 2.07 mmol) and conc. HCl (0.10 mL) in MeOH (6 mL) was refluxed for 8 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure to give the crude material that was redissolved into EtOAc. The organic layer was washed with water, dried over MgSO4, filtered, and concentrated under reduced pressure to give the crude material that was purified by silica gel flash column chromatography (100% hexanes to 10 to 20 to 30 to 50% EtOAc in hexanes) to afford 72 mg (17%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101639B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-5bf7c72c96054de0b99e95185020bacf |
| Source note | uspto-grants-2012_01 |