HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 6-(N-ethyl-N-(2-aminobenzyl)amino)-pyridazine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-ethyl-N-(2-aminobenzyl)amine | HCID 10329442 | — |
| Reactant | 6-Chloropyridazine-3-carboxamide | HCID 12577557 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(N-ethyl-N-(2-aminobenzyl)amino)-pyridazine-3-carboxamide | HCID 22675468 | 39.2% |
Reaction Steps
N-Ethyl-N-(2-aminobenzyl)amine (707 mg, 4.7 mmol) in DMF (11 ml) was treated with 6-chloropyridazin-3-amide (4.7 mmol) followed by diisopropylethylamine (15.4 mol) and the reaction stirred at 140° under argon for 24 hours. The reaction was evaporated in vacuo (cold-finger) and the residue partitioned between water and ethyl acetate. The combined organic extracts were dried and evaporated to give a brown gum. The gum was purified by medium pressure chromatography to give 6-(N-ethyl-N-(2-aminobenzyl)amino)-pyridazine-3-carboxamide (500 mg, 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06057345 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-901bac4e2f484146b16fce4e0e93c1f4 |
| Source note | uspto-grants-2000_05 |