HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N,N-trimethyl-1,1-bis(1-methylethoxy)amine → Methyl 1-[2-fluoro-4-(trifluoromethoxy)phenyl]-5-methoxy-4-oxo-1,4-dihydropyridazine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N,N-trimethyl-1,1-bis(1-methylethoxy)amine | HCID 87682 | — |
| Reactant | HCID 178496283 | HCID 178496283 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 1-[2-fluoro-4-(trifluoromethoxy)phenyl]-5-methoxy-4-oxo-1,4-dihydropyridazine-3-carboxylate | HCID 59436184 | 86% |
Reaction Steps
A solution of methyl 2-{[2-fluoro-4-(trifluoromethoxy)phenyl]hydrazono}-4-methoxy-3-oxobutanoate (3.8 g, 11 mmol) and N,N-dimethylformamide diisopropyl acetal (9.5 mL, 54 mmol) in toluene (60 mL) was refluxed for 5 h. The mixture was concentrated under reduced pressure. The residue was diluted with AcOEt, washed with water and brine. The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure. The residue was chromatographed on silica gel (10/90-100/0 AcOEt/hexane) to give the title compound (3.4 g, 86% yield) as pale yellow crystals: 1H NMR (300 MHz, CDCl3): δ ppm 3.91 (3H, s), 3.97 (3H, s), 7.17-7.25 (2H, m), 7.68-7.76 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513251B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-1cb235d78df048cd9d744b630d2b4276 |
| Source note | uspto-grants-2013_08 |