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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399354Generated: November 2, 2026

Benzylamine → 3-Benzylamino-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazine

https://huagongshe.com/reaction/2399354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant3-Chloro-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazineHCID 19385500—
Product3-Benzylamino-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazineHCID 1938548392.4%

Reaction Steps

14 g (46 mmol) of 3-chloro-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazine are heated in 74 g (0.69 mol) of benzylamine at 200° C. for 3 hours. The mixture is subsequently poured onto ice and extracted with dichloromethane, and the organic phase is dried with potassium carbonate and then concentrated. Petroleum ether (b.p. 50°-70° C.) is added to the residue, and the resulting precipitate is filtered off with suction and crystallized from ethyl acetate/cyclohexane. 15.9 g (92.4%) of 3-benzylamino-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazine of m.p. 116° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05449676
Source datasetuspto-grants-1995_09
ORD IDord-9d574a73ca0645858722c352ff47eb81
Source noteuspto-grants-1995_09