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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375885Generated: October 31, 2026

Dimethyl Sulfoxide → 1-ethyl-6-bromo-N-(cyclohexylmethyl)-1H-pyrazolo[3,4-b]quinolin-4-amine

https://huagongshe.com/reaction/375885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantAmmonium HydroxideHCID 14923—
ReactantCyclohexanemethylamineHCID 76688—
Reactant1-ethyl-4-chloro-6-bromo-1H-pyrazolo[3,4-b]quinolineHCID 19592219—
SolventWaterHCID 962—
Product1-ethyl-6-bromo-N-(cyclohexylmethyl)-1H-pyrazolo[3,4-b]quinolin-4-amineHCID 2121772198.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 1-ethyl-4-chloro-6-bromo-1H-pyrazolo[3,4-b]quinoline (6.5 g, 0.021 mol), cyclohexanemethylamine (5.46 g, 0.042 mol) and DMSO (20 ml) was heated at 110° C. overnight. The reaction mixture was cooled, poured into water and basified with NH4OH. The mixture was extracted with CH2Cl2 (2×100 ml) and the combined CH2Cl2 extracts were washed with brine, then evaporated to about 20 ml. The solution was purified by column chromatography on silica gel eluting with ethyl acetate to afford 8.0 g (98.8%) of 1-ethyl-6-bromo-N-(cyclohexylmethyl)-1H-pyrazolo[3,4-b]quinolin-4-amine, m.p. 158°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05488055
Source datasetuspto-grants-1996_01
ORD IDord-c8a961def5b94fb1b79515683903592c
Source noteuspto-grants-1996_01