HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 4-Bromo-6-chloro-5-methylpyridazin-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-Chloro-5-methylpyridazin-3-amine | HCID 12353663 | — |
| Reactant | 6-Chloro-4-methylpyridazin-3-amine | HCID 12353664 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Bromo-6-chloro-5-methylpyridazin-3-amine | HCID 59624331 | — |
Reaction Steps
The mixture of 6-chloro-5-methylpyridazin-3-amine and 3-chloro-5-methylpyridazin-6-amine (1.45 g, 10 mmol) from 1a and NaHCO3 (2.1 g, 25 mmol) were suspended in MeOH (20 mL) and treated with Br2 (0.57 mL, 11 mmol). The mixture was stirred at room temperature for 4 h, then filtered. The filtrate was condensed in vacuo. The resulting residue was resuspended in EtOAc (100 mL) and washed sequentially with sat. aqueous NaHCO3 solution (2×20 mL) and aqueous NaCl solution (1×20 mL). The solution was dried over MgSO4. The solvent was removed in vacuo to give crude 4-bromo-6-chloro-5-methylpyridazin-3-amine (1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723336B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-e3c58a78953b4cfb8d08e35ebd2f641b |
| Source note | uspto-grants-2010_05 |