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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455944Generated: October 31, 2026

Formic Acid → 6-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]pyridazine-3-carboxylic acid

https://huagongshe.com/reaction/1455944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantIsopropanolHCID 3776—
ReactantSodium HydroxideHCID 14798—
Reactant6-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]pyridazine-3-carboxamideHCID 18693221—
SolventWaterHCID 962—
Product6-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]pyridazine-3-carboxylic acidHCID 984617097.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 6-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]pyridazine-3-carboxamide (61.7 g), sodium hydroxide (28 g) and isopropanol (400 ml) was heated at reflux for 1 hour. The mixture was cooled to 70° C. and water (800 ml) was added over 30 minutes. The mixture was acidified to pH 3-4 with a solution of formic acid (41.5 ml) in water (200 ml) over 30 minutes, at 25°-30° C. The mixture was cooled to 10° C., the produce filtered off, washed with water and dried to give 6-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]pyridazine-3-carboxylic acid (60.2 g, 97.2% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843942
Source datasetuspto-grants-1998_12
ORD IDord-d78a3dbaa9874e80911ca6ad1894cd4a
Source noteuspto-grants-1998_12