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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458742Generated: November 1, 2026

Hydrochloric Acid → 1-ethyl-3-methyl-N-(phenylmethyl)-1H-pyrazolo[3,4-b]quinolin-4-amine

https://huagongshe.com/reaction/1458742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzylamineHCID 7504—
ReactantAmmonium HydroxideHCID 14923—
Reactant1-ethyl-3-methyl-4-chloro-1H-pyrazolo[3,4-b]quinolineHCID 19592234—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-ethyl-3-methyl-N-(phenylmethyl)-1H-pyrazolo[3,4-b]quinolin-4-amineHCID 7008746266.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-ethyl-3-methyl-4-chloro-1H-pyrazolo[3,4-b]quinoline (1.0 g, 4.3 mmol), DMSO (3 ml) and benzylamine (0.98 ml, 9 mmol) is heated at 80° C. overnight. The reaction mixture is poured into water (100 ml), then NH4OH (0.5 ml) is added. The mixture is extracted with CH2Cl2 (200 ml) and the CH2Cl2 is concentrated to about 20 ml, and then this solution is purified by column chromatography on silica gel, followed by high pressure liquid chromatography eluting with 20% ethyl acetate/hexane to afford the product as the free base. The free base is dissolved in CH2Cl2 (20 ml) and treated with ethereal HCl. The mixture is evaporated and the residue is crystallized from ether to afford 0.9 g of 1-ethyl-3-methyl-N-(phenylmethyl)-1H-pyrazolo[3,4-b]quinolin-4-amine.HCl, as an off white solid, m.p. 228°-231° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852035
Source datasetuspto-grants-1998_12
ORD IDord-2413acdfce3f4f25b7be5b592d303158
Source noteuspto-grants-1998_12