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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375867Generated: October 30, 2026

Epichlorohydrin → HCID 86749231, compound

https://huagongshe.com/reaction/375867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 9818690HCID 9818690—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 86749231HCID 86749231—

Reaction Steps

A mixture of 1-ethyl-6-hydroxy-N-(cyclohexylmethyl)-1H-pyrazolo[3,4-b]quinolin-4-amine (6 g), KOH (5 g), and DMSO (70 ml) was stirred for 30 minutes and then epichlorohydrin (1.5 ml) was added. The reaction mixture was stirred overnight and then was partitioned between CH2Cl2 and water. The organic layer was then separated, dried and evaporated to dryness. The residue was purified by column chromatography on silica gel eluting with ethyl acetate, followed by crystallization from hexane/ether to afford 1.0 g of 1-ethyl-6-(2,3-epoxypropoxy)-N-(cyclohexylmethyl)-1H-pyrazolo[3,4-b]quinolin-4-amine, m.p. 160°-163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05488055
Source datasetuspto-grants-1996_01
ORD IDord-578cf4522a0b475fa051651aca3fb270
Source noteuspto-grants-1996_01