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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399355Generated: October 30, 2026

Hydrochloric Acid → HCID 19385486, compound

https://huagongshe.com/reaction/2399355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCyclohexeneHCID 8079—
Reactant3-Benzylamino-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazineHCID 19385483—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 19385486HCID 1938548642.1%

Reaction Steps

15 g (40 mmol) of 3-benzylamino-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazine are heated to reflux in a mixture of 100 ml of glacial acetic acid, 6.5 ml of concentrated hydrochloric acid, 9.8 g (0.12 mol) of cyclohexene and 3 spatula tips of Pd/C (10 percent) for 4 hours. 9.8 g of cyclohexene and Pd/C are added once again, and boiling is continued for 16 hours. The catalyst is filtered off, the solution is diluted with 1 l of water and neutralized with concentrated ammonia, and the resulting precipitate is filtered off with suction. The product is purified by chromatography on silica gel with dichloromethane. 4.8 g (42.1%) of 3-amino-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazine of m.p. 207° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05449676
Source datasetuspto-grants-1995_09
ORD IDord-21b5bd2982ed441188bf3ff9634a9478
Source noteuspto-grants-1995_09