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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769664Generated: October 31, 2026

3-Chloro-6-methoxypyridazine → 4-(6-Methoxypyridazin-3-yl)benzaldehyde

https://huagongshe.com/reaction/1769664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-6-methoxypyridazineHCID 74403—
Reactant3-tert-Butyl-6-chloropyridazineHCID 13499979—
Reactant5-Chloro-1-methylpyridin-2(1H)-oneHCID 13651728—
ReactantHCID 19082048HCID 19082048—
SolventPyridineHCID 1049—
Product4-(6-Methoxypyridazin-3-yl)benzaldehydeHCID 15045326—

Reaction Steps

The following compounds were synthesized in the same procedures as in the Preparation Example 2 except for using 2-chloropyridazine, 5-chloro-1-methyl-1,2-dihydro-2-oxopyridine, 3-chloro-6-tert-butylpyridazine, 5-chloro-2-(3,4-dimethoxyphenyl)methyl)pyridine respectively instead of 3-chloro-6-methoxypyridazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05382595
Source datasetuspto-grants-1995_01
ORD IDord-2d875041f53744c98d870d3ffe4ceab9
Source noteuspto-grants-1995_01