HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → 1456534-36-3
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | (4,6-Dichloropyrimidin-5-yl)acetaldehyde | HCID 13989292 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1456534-36-3 | HCID 89816033 | 54% |
Reaction Steps
To a stirred solution of 2-(4,6-dichloropyrimidin-5-yl)acetaldehyde (600 mg) in dry MeCN (10 mL), methyl hydrazine (154 mg) and sodium acetate (514 mg) were added. The reaction mixture was stirred at room temperature for 3 hours and solvents were removed under reduced pressure. The resulting oil was diluted with ethyl acetate (50 mL), washed with water (10 mL) and brine (10 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated. The resulting crude product was purified by column chromatography using EtOAc/CHCl3 (0.4:9.6) as eluent to afford 5-chloro-1-methyl-1,4-dihydropyridazino[3,4-d]pyrimidine (310 mg) as white solid. 1H NMR (DMSO-d6): δ 3.34 (s, 3H), 3.53-3.54 (d, 2H), 6.91-6.93 (t, 1H), 8.38 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193725B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-ac1b36725a724a6aa05f1d58a5e685f2 |
| Source note | uspto-grants-2015_11 |