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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375850Generated: October 27, 2026

Dimethyl Sulfoxide → 1-ethyl-N-[[4-(methylthiomethoxycarbonyl)cyclohexyl]methyl]-1H-pyrazolo[3,4-b]quinolin-4-amine

https://huagongshe.com/reaction/375850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant1-ethyl-4-chloro-1H-pyrazolo[3,4-b]quinolineHCID 15816908—
ReactantHCID 178511262HCID 178511262—
Product1-ethyl-N-[[4-(methylthiomethoxycarbonyl)cyclohexyl]methyl]-1H-pyrazolo[3,4-b]quinolin-4-amineHCID 9822982—

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 4-chloro-1-ethyl-1H-pyrazolo[3,4-b]quinoline (3 g), DMSO (9 ml) and trans-4-(aminomethyl)cyclohexane carboxylic acid (4.1 g) was heated at 180° C. overnight. The reaction mixture was then partitioned between CH2Cl2 and water, the layers were separated and the aqueous layer was extracted with CH2Cl2. The organic layers were combined, washed with water, dried over Na2SO4, and evaporated. The residue was purified by column chromatography on silca gel to afford an oil which was crystallized from ether/hexane and then recrystallized from ether/hexane to afford 1-ethyl-N-[[4-(methylthiomethoxycarbonyl) cyclohexyl]methyl]-1H-pyrazolo[3,4-b]quinolin-4-amine, m.p. 135°-136° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05488055
Source datasetuspto-grants-1996_01
ORD IDord-b91da9fbc55d42aa85ba9406b896131b
Source noteuspto-grants-1996_01