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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399358Generated: October 30, 2026

HCID 19385492, compound → HCID 19385504, compound

https://huagongshe.com/reaction/2399358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19385492HCID 19385492—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductHCID 19385504HCID 1938550446.1%

Reaction Steps

10 g (36 mmol) of 3-hydrazino-6-[4-methoxy-3-(1-methylethoxy)phenyl]pyridazine are hydrogenated in 100 ml of methanol in the presence of 1 g of Raney nickel with hydrogen under atmospheric pressure at room temperature while stirring efficiently. Starting material is no longer detectable after 4 hours. The solution is filtered to remove catalyst and concentrated in vacuo, and the residue is crystallized from isopropanol/cyclohexane. 4.3 g (46%) of 3-amino-6-[4-methoxy-3-(1-methylethoxy)phenyl]pyridazine of m.p. 184° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05449676
Source datasetuspto-grants-1995_09
ORD IDord-2a9bc8d5480745b89faaf6320146dc8d
Source noteuspto-grants-1995_09