HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichloropropene → Butyl 6-[N-(5-bromo-2-(2-chloroprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichloropropene | HCID 6565 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | butyl 6-[N-(5-bromo-2-hydroxybenzyl)-N-ethylamino]pyridazine-3-carboxylate | HCID 22622486 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Butyl 6-[N-(5-bromo-2-(2-chloroprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazine-3-carboxylate | HCID 18693232 | 72% |
Reaction Steps
Butyl 6-[N-(5-bromo-2-hydroxybenzyl)-N-ethylamino]pyridazine-3-carboxy late (reference example 11) (0.28 g, 0.69 mmol) in DMF (4 ml) was treated with potassium carbonate (0.28 g, 2.05 mmol) followed by 2,3-dichloro-1-propene (168 mg, 140 μl, 1.4 mmol) and the mixture stirred at ambient temperature over the weekend. The mixture was evaporated, in vacuo, to dryness, presorbed to 1.5 g silica and purified by MPLC to give the title compound as a colourless gum (0.24 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06100258 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-60ea28f0b7c94ab2aeda92774b31d8ab |
| Source note | uspto-grants-2000_08 |