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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199056Generated: October 31, 2026

4-Methoxy-N-[2-nitro-4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl]benzamide → N-[2-Amino-4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl]-4-methoxy-benzamide

https://huagongshe.com/reaction/2199056

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-N-[2-nitro-4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl]benzamideHCID 13850880—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-[2-Amino-4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl]-4-methoxy-benzamideHCID 13850881—

Reaction Steps

9.8 gm of 5-methyl-6-[3-nitro-4-(4-methoxy-benzoylamino)-phenyl]-3-oxo-4,5-dihydro-2H-pyridazine were dissolved in 1000 ml of ethanol and hydrogenated for 24 hours at room temperature with a hydrogen pressure of 5 bar in the presence of 1 gm of 10% palladium charcoal. The obtained precipitate was suction filtered and used in the next step without removing the catalyst. A further fraction of the product can be obtained from the mother liquors.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04361563
Source datasetuspto-grants-1982_11
ORD IDord-16957286d7e142388c4251bff0d3b389
Source noteuspto-grants-1982_11