HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → Pyridazine-3-carboximidamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Pyridazine-3-carbonitrile | HCID 13642940 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Pyridazine-3-carboximidamide hydrochloride | HCID 18756080 | — |
Reaction Steps
To a solution of compound 1-c (2.7 g, 25.7 mmol) in MeOH (25 mL) was added sodium methoxide (139 mg, 0.257 mmol). The reaction was stirred at room temperature overnight when ammonium chloride (1.65 g, 30.8 mmol) was added. The reaction was refluxed for 3 h, cooled to room temperature and concentrated to afford the crude product of 1-d (3.8 g, 93%). 1H NMR (300 MHz, DMSO-d6) δ 9.38 (dd, J=1.5, 5.1 Hz, 1H), 8.30 (dd, J=1.5, 8.7 Hz, 1H), 7.92 (dd, J=5.1, 8.4 Hz, 1H). LC-MS: (M+H)+123.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006433B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-1624702bb73643f7bb9cdbb8cbb22e3b |
| Source note | uspto-grants-2015_04 |