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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249418Generated: November 2, 2026

4-carboxy-2-(4-chlorobenzyl)-6-(2,3-dihydro-1-benzofuran-5-yl)-2H-pyridazin-3-one → 2-(4-chlorobenzyl)-6-(2,3-dihydro-1-benzofuran-5-yl)-4-hydroxymethyl-2H-pyridazin-3-one

https://huagongshe.com/reaction/2249418

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-carboxy-2-(4-chlorobenzyl)-6-(2,3-dihydro-1-benzofuran-5-yl)-2H-pyridazin-3-oneHCID 23094129—
Reactant2-(4-fluorobenzyl)-6-(2,3-dihydro-1-benzofuran-5-yl)-4-(4-methyl-1-piperazinyl)methyl-2H-pyridazin-3-oneHCID 23094132—
Product2-(4-chlorobenzyl)-6-(2,3-dihydro-1-benzofuran-5-yl)-4-hydroxymethyl-2H-pyridazin-3-oneHCID 2309412532.7%

Reaction Steps

The general procedure of Example 1 (4) was repeated by use of 4-carboxy-2-(4-chlorobenzyl)-6-(2,3-dihydro-1-benzofuran-5-yl)-2H-pyridazin-3-one, to thereby yield the title compound as a pale yellow powder (yield: 32.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314877B2
Source datasetuspto-grants-2008_01
ORD IDord-d39d9756a45d42efab4a5eb0daf2bc72
Source noteuspto-grants-2008_01