HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,6-Dichloropyridazine → 6-Chloro-N-methylpyridazin-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | Monomethylamine methanol | HCID 57454252 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Chloro-N-methylpyridazin-3-amine | HCID 588540 | 104.7% |
Reaction Steps
3,6-Dichloropyridazine (107, 500 mg, 3.36 mmol) was slowly added to a 2.0 M methylamine methanol solution (NH2Me in MeOH, 5 mL, 10 mmol) and stirred at room temperature for 24 hours. Water was added to the reaction mixture, and organic compounds were extracted with ethyl acetate. The recovered organic solution was washed with an aqueous solution of saturated sodium chloride and evaporated after a treatment with sodium sulfate. Purification was performed by column chromatograph to give the target compound 3-(N-monomethylamino)-6-chloropyridazine (108e, 505 mg, 88%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08497260B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-171ec25a3f954b868203a18a0508ed80 |
| Source note | uspto-grants-2013_07 |