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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634107Generated: November 2, 2026

2-Methylbenzonitrile → [4-(5-Ethyl-3-pyridin-3-yl-pyrazol-1-yl)phenyl]-(2-methylbenzyl)amine

https://huagongshe.com/reaction/1634107

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylbenzonitrileHCID 10721—
Reactant1-(4-Aminophenyl)-3-(3-pyridyl)-5-ethylpyrazoleHCID 18677094—
CatalystNickelHCID 935—
SolventAcetic AcidHCID 176—
Product[4-(5-Ethyl-3-pyridin-3-yl-pyrazol-1-yl)phenyl]-(2-methylbenzyl)amineHCID 984222485%

Reaction Steps

A slurry of Raney Ni (200 mg, 50% in water) was added to a solution 5-ethyl-3-(3-pyridyl)-1-(4′-aminophenyl)pyrazole (500 mg, 1.89 mmol) and o-tolunitrile (0.27 mL, 1.2 equiv.) in glacial acetic acid (20 mL), and the mixture was stirred under hydrogen at 40 psi for 7.5 h. The reaction mixture was filtered through diatomaceous earth, diluted with water, extracted with ethyl acetate, washed with brine, dried (Na2SO4) and concentrated. Chromatography on silica gel (hexane/ethyl acetate=1:1) gave the title compound (595 mg, 85%). 1H-NMR (CDCl3): 1.30 (t, J=7.5 Hz, 3H), 2.42 (s, 3H), 2.69 (q, J=7.5 Hz, 2H), 3.95-4.25 (bs, 1H), 4.36 (s, 2H), 6.58 (s, 1H), 6.72 (d, J=8.7 Hz, 1H), 7.21-7.41 (m, 6H), 8.21 (dd, J=1.6, 6.3 Hz, 1H), 8.56 (d, J=4.1 Hz, 1H), 9.10 (d, J=1.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506747B1
Source datasetuspto-grants-2003_01
ORD IDord-65ee236e77d24c0584e535b733a23dd9
Source noteuspto-grants-2003_01