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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170262Generated: November 3, 2026

Sulfuric Acid → 2-((4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)phenoxy)methyl)quinoline

https://huagongshe.com/reaction/1170262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantMethylhydrazineHCID 6061—
Reactant2-((4-(4-pyridin-4-yl-1H-pyrazol-3-yl)phenoxy)methyl)quinolineHCID 11610553—
SolventEthanolHCID 702—
Product2-((4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)phenoxy)methyl)quinolineHCID 1158193656%

Reaction Steps

To a solution of 2-[-4-(4-Pyridin-4-yl-2H-pyrazol-3-yl)-phenoxymethyl}-quinoline (1.72 g) in ethanol (20 ml) was added methyl hydrazine (3.5 ml, 1.5 eq.) and concentrated sulfuric acid (0.1 ml). The reaction mixture was stirred 1 h at ambient temperature and solvent evaporated. The reaction mixture was partitioned between methylene chloride and saturated sodium bicarbonate. The layers were separated and the organic layer dried magnesium sulfate, filtered and concentrated. Preparative HPLC chromatography provided the title compound (major isomer) as a clear oil (0.97 g, 56%). 1H NMR (400 MHz, CDCl3) δ 8.44 (d, J=5.0 Hz, 2H), 8.17 (d, J=8.7 Hz, 1H), 8.05 (d, J=8.3 Hz, 1H), 7.81 (d, J=7.9 Hz, 1H), 7.70 (m, 1H), 7.66 (d, J=8.7 Hz, 1H), 7.54 (s, 1H), 7.53 (m, 1H), 7.37 (d, J=8.7 Hz, 2H) 7.15 (d, J=5.0, 2H), 7.00 (d, J=8.7 Hz, 2H), 5.38 (s, 2H), 3.93 (s, 3H); MS: (M+H m/z=393.3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825254B2
Source datasetuspto-grants-2010_11
ORD IDord-daae702408f848f3b8ca287d2cb90da7
Source noteuspto-grants-2010_11