HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-imidazo[1,2-b]pyridazin-7-yl-N-methylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(6-Amino-1,6-dihydro-pyridazin-4-yl)-N-methyl-benzamide | HCID 59443495 | — |
| Product | 3-imidazo[1,2-b]pyridazin-7-yl-N-methylbenzamide | HCID 59443501 | — |
Reaction Steps
3-(6-Amino-1,6-dihydro-pyridazin-4-yl)-N-methyl-benzamide (1 eq, 1.07 mmol, 245 mg) is added to a solution of chloroacetic aldehyde (5 eq, 5.4 mmol, 0.69 ml) in EtOH (15 ml). NaHCO3 (2 eq, 2.15 mmol, 180 mg) is then added and the reaction mixture is heated at reflux for 17 h. The solvent is then removed in vacuo and the product is purified by flash column chromatography eluting with 9:1 DCM/MeOH to afford 3-imidazo-[1,2-b]-pyridazin-7-yl-N-methyl-benzamide as an orange solid; [M+H]+=253
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143253B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-fa0f24d095c74567951526d3fda4b365 |
| Source note | uspto-grants-2012_03 |