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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382269Generated: October 31, 2026

3-Cyclohexylcarbonyl-4-chloro-8-methoxyquinoline → 3-Cyclohexylcarbonyl-4-(2-methylphenylamino)-8-methoxyquinoline

https://huagongshe.com/reaction/1382269

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclohexylcarbonyl-4-chloro-8-methoxyquinolineHCID 11722542—
SolventO-ToluidineHCID 7242—
Solvent1,4-DioxaneHCID 31275—
Product3-Cyclohexylcarbonyl-4-(2-methylphenylamino)-8-methoxyquinolineHCID 1024884618.2%

Reaction Steps

3-cyclohexylcarbonyl-4-chloro-8-methoxyquinoline (5.0 g, 0.017 mol) was heated under reflux in a mixture of 1,4-dioxan (50 ml) and o-toluidine (2.0 ml) for 2 hours. The reaction mixture was evaporated and the residue dissolved in dichloromethane, washed with sodium hydrogen carbonate solution and brine. The organic solution was dried, evaporated and chromatographed (silica gel, dichloromethane) to affort an oil, which on trituration with hexane-ether gave 3-cyclohexylcarbonyl-4-(2-methylphenylamino)-8-methoxyquinoline as yellow crystals (0.58 g, 9.4%) m.p. 115°-7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04806549
Source datasetuspto-grants-1989_02
ORD IDord-57226a1bcbd147a793daa544ce16ad2b
Source noteuspto-grants-1989_02