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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249421Generated: October 31, 2026

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

https://huagongshe.com/reaction/2249421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-chlorobenzyl)-6-(2,3-dihydro-1-benzofuran-5-yl)-4-methanesulfonyloxymethyl-2H-pyridazin-3-oneHCID 23094103—
ReactantHCID 23094117HCID 23094117—
Reactantp-Chlorocinnamyl chlorideHCID 53728250—
Product4-carboxy-2-(4-chlorocinnamyl)-6-(2,3-dihydro-1-benzofuran-5-yl)-2H-pyridazin-3-oneHCID 6930888044.4%

Reaction Steps

The general procedure of Example 1 (3) was carried out by use of 6-(2,3-dihydro-1-benzofuran-5-yl)-4-methoxycarbonyl-2H-pyridazin-3-one and 4-chlorocinnamyl chloride, to thereby yield the title compound as an orange powder (yield: 44.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314877B2
Source datasetuspto-grants-2008_01
ORD IDord-6b465427e86e4622bcbd46b317d3a587
Source noteuspto-grants-2008_01