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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721850Generated: October 25, 2026

2-Methylhexanoic Acid → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N'-(2-methylhexanoyl)thiourea

https://huagongshe.com/reaction/721850

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylhexanoic AcidHCID 20653—
ReactantThionyl ChlorideHCID 24386—
Reactant2-methylhexanoyl ChlorideHCID 3458543—
Reactant4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
Reactant2-Methylhexanoyl isothiocyanateHCID 21890727—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductN-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N'-(2-methylhexanoyl)thioureaHCID 2189097868%

Reaction Conditions

Temperature100 °C

Reaction Steps

Toluene (20 ml) and thionyl chloride (1 ml) were added to commercially available 2-methylhexanoic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 2-methylhexanoyl isothiocyanate was prepared using the resultant 2-methylhexanoyl chloride as a starting compound according to the description of the literature. 2-Methylhexanoyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 4-[(6,7-Dimethoxy-4-quinolyl)oxy]aniline (50 mg), toluene (5 ml), and ethanol (1 ml) were added to the solution, and the mixture was stirred at room temperature for 2 hr. The reaction solution was concentrated, and the residue was purified by chromatography on silica gel using chloroform/acetone for development to give the title compound (54 mg, yield 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-3b19a9eb7505429ea0122b6443f4f411
Source noteuspto-grants-2006_11