HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N'-Hydroxy-6-methyl-3-pyridazinecarboximidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 6-Methylpyridazine-3-carbonitrile | HCID 13642941 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N'-Hydroxy-6-methyl-3-pyridazinecarboximidamide | HCID 136347704 | — |
Reaction Steps
3-Cyano-6-methyl pyridazine (U.S. Pat. No. 5,914,319) (0.77 g, 6.4 mmol) was dissolved in methanol (20 mL), then hydroxylamine hydrochloride (0.66 g, 9.6 mmol) and triethylamine (1.3 mL, 9.6 mmol) were added and the mixture was stirred at room temperature overnight. The mixture was chilled in an ice-bath, then the solid was collected by filtration, washed with methanol and dried to give the title compound as a pale yellow solid (0.84 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06821972B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-cda37a2c2645428fb511e980785d23db |
| Source note | uspto-grants-2004_11 |