HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Bromo-N-(6-methyl-pyridazin-3-yl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 6-Methylpyridazin-3-amine | HCID 87712 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Bromo-N-(6-methyl-pyridazin-3-yl)-acetamide | HCID 67310801 | — |
Reaction Steps
A solution of bromoacetyl bromide (0.22 mL) in dry CHCl3 (4 mL) was added slowly to a suspension of 3-amino-6-methylpyridazine (0.24 g) and triethylamine (0.47 mL) in dry CHCl3 (45 mL) at room temperature. The brown mixture was allowed to stir for 3.5 hr, then quenched with H2O (1.5 mL) and stirred for 20 mins before concentrating under reduced pressure to a brown solid. The crude product was purified by silica gel chromatography eluting with 1-2% MeOH/dichloromethane. The relevant fractions were combined and evaporated to give the title compound (0.20 g) as a pinkish/beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08329729B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-f936bb35d18b4f92b12d235e0b7d0eff |
| Source note | uspto-grants-2012_12 |