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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604378Generated: October 31, 2026

Sodium Hydroxide → 6-[N-(5-Bromo-2-hydroxybenzyl)-N-ethylamino]pyridazine-3-carboxylic acid

https://huagongshe.com/reaction/1604378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantbutyl 6-[N-(5-bromo-2-hydroxybenzyl)-N-ethylamino]pyridazine-3-carboxylateHCID 22622486—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product6-[N-(5-Bromo-2-hydroxybenzyl)-N-ethylamino]pyridazine-3-carboxylic acidHCID 2262253373.8%

Reaction Steps

A solution of butyl 6-[N-(5-bromo-2-hydroxybenzyl)-N-ethylamino]pyridazine-3- carboxylate (reference example 3) (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 dried (MgSO4) to give the title compound as a white solid (0.26 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994353
Source datasetuspto-grants-1999_11
ORD IDord-5c7f990d763c45f98f9176abf77fbe2d
Source noteuspto-grants-1999_11