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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977134Generated: October 31, 2026

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

https://huagongshe.com/reaction/977134

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) was heated at 80° C. overnight. The reaction mixture was poured into water (100 ml), then NH4OH (0.5 ml) was added. The mixture was extracted with CH2Cl2 (200 ml) and the CH2Cl2 was concentrated to about 20 ml and then this solution was 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 was dissolved in CH2Cl2 (20 ml) and treated with ethereal HCl. The mixture was evaporated and the residue was 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 numberUS05614530
Source datasetuspto-grants-1997_03
ORD IDord-0f8158c75c7a442a865c33f791523301
Source noteuspto-grants-1997_03