HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 6-[N-(5-Bromo-2-hydroxybenzyl)-N-ethylamino]pyridazine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | butyl 6-[N-(5-bromo-2-hydroxybenzyl)-N-ethylamino]pyridazine-3-carboxylate | HCID 22622486 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-[N-(5-Bromo-2-hydroxybenzyl)-N-ethylamino]pyridazine-3-carboxylic acid | HCID 22622533 | 73.8% |
Reaction Steps
A solution of butyl 6-[N-(5-bromo-2-hydroxybenzyl)-N-ethylamino]pyridazine-3-carboxylate (reference example 11) (0.36 g, 1.0 mmol) in THF (4 ml) and methanol (4 ml) was treated with aqueous sodium hydroxide 1N (4 ml) and allowed to stand at ambient temperature for 1.5 hours. The reaction was evaporated to a small volume, diluted with water and acidified with acetic acid. After standing for 18 hours, the precipitate was filtered, washed with water and ether, and air dried to give the title compound as a white solid (0.26 g, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06100258 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-2c3bf1ec83ef4b888d5e2acb7232c7f5 |
| Source note | uspto-grants-2000_08 |