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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586151Generated: October 31, 2026

Epichlorohydrin → HCID 86749231, compound

https://huagongshe.com/reaction/1586151

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) is stirred for 30 minutes and then epichlorohydrin (1.5 ml) is added. The reaction mixture is stirred overnight and then is partitioned between CH2Cl2 and water. The organic layer is then separated, dried and evaporated to dryness. The residue is 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 numberUS05942520
Source datasetuspto-grants-1999_08
ORD IDord-2002e0dc0e8b45efaf67369481552e7a
Source noteuspto-grants-1999_08