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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372714Generated: November 1, 2026

Ammonium Hydroxide → Ethyl 3-(5-methyl-6-phenyl-3-pyridazinyl)carbazate

https://huagongshe.com/reaction/372714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantEthyl 3-[6-(p-bromophenyl)-5-methyl-3-pyridazinyl]carbazateHCID 20326503—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductEthyl 3-(5-methyl-6-phenyl-3-pyridazinyl)carbazateHCID 20326540—

Reaction Steps

A 4.0 g. portion of ethyl 3-[6-(p-bromophenyl)-5-methyl-3-pyridazinyl]carbazate and 0.9 g. of 10% palladium on carbon catalyst in 100 ml. of ethanol and 50 ml. of ammonium hydroxide is shaken under 40 lb. of hydrogen pressure for 4 hours with external heating of the bottle by means of a heated jacket. The reaction mixture is suction filtered and the filtrate is concentrated to a light yellow oil which is scratched with petroleum ether to give a white solid, m.p. 142°-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04092311
Source datasetuspto-grants-1978_05
ORD IDord-904395718bfe4d76b2ba1261f441db63
Source noteuspto-grants-1978_05