HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 6-Iodoimidazo[1,2-b]pyridazine-2-carboxylate → 6-iodo-N-methylimidazo[1,2-b]pyridazine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 6-Iodoimidazo[1,2-b]pyridazine-2-carboxylate | HCID 51063906 | — |
| Reactant | Methylamine tetrahydrofuran | HCID 66615946 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-iodo-N-methylimidazo[1,2-b]pyridazine-2-carboxamide | HCID 57441026 | 71.6% |
Reaction Steps
To a suspension of ethyl 6-iodoimidazo[1,2-b]pyridazine-2-carboxylate (4.5 g, 14.8 mmol) in methanol (13.5 mL) was added dropwise a solution of methylamine/tetrahydrofuran (2 mol/L, 37.1 mL, 74.2 mmol), and the mixture was stirred at room temperature for 96 hr. The solvent was evaporated under reduced pressure, and the residue was washed with ethyl acetate, saturated brine and water to give the title compound (3.2 g, 71%) as a dark brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08034812B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-60a707966e3f4d2a9b068881a61dc94f |
| Source note | uspto-grants-2011_10 |