HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-Chloro-1-mesityl-6-methyl-1,6-dihydro-7H-pyrrolo[2,3-d]pyridazin-7-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-chloro-1-mesityl-1,6-dihydro-7H-pyrrolo[2,3-d]pyridazin-7-one | HCID 67267604 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-1-mesityl-6-methyl-1,6-dihydro-7H-pyrrolo[2,3-d]pyridazin-7-one | HCID 67267127 | 98% |
Reaction Steps
A mixture of 4-chloro-1-mesityl-1,6-dihydro-7H-pyrrolo[2,3-d]pyridazin-7-one (0.43 g, 1.5 mmol), MeI (0.103 ml, 1.65 mmol), potassium carbonate (0.41 g, 3.0 mmol) and DMF (5 ml) was stirred at room temperature for 19 hours. The mixture was diluted with water (50 ml) and extracted with ethyl acetate (50 ml). The extract was washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with hexane/ethyl acetate (3:1) to give 0.38 g (98%) of the title compound as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897607B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-3ee7d72ded58460f97e972edf5074821 |
| Source note | uspto-grants-2011_03 |