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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980827Generated: October 31, 2026

2-Chloro-6,7-dimethoxy-4-quinazolinamine → HCID 20220996, compound

https://huagongshe.com/reaction/980827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6,7-dimethoxy-4-quinazolinamineHCID 90235—
Reactant5,5-Dimethyl-3-piperazin-1-yl-cyclohex-2-enoneHCID 648131—
SolventIsoamyl AlcoholHCID 31260—
ProductHCID 13520910HCID 1352091078%
ProductHCID 20220996HCID 20220996204.6%

Reaction Steps

A mixture of 4.8 g (0.02 mol) of 2-chloro-4-amino-6,7-dimethoxyquinazoline, 4.6 g (0.022 mol) of (3-oxo-5,5-dimethyl-1-cyclohexen-1-yl)-piperazine and 80 ml of isoamyl alcohol is boiled under reflux for 3 hours, with stirring. During the reaction time, the monohydrochloride precipitates. The mixture is left to stand overnight and the crystals are filtered off with suction. After washing with 40 ml of isoamyl alcohol and twice with in each case 40 ml of absolute acetone and 40 ml of absolute ether and drying, 7.1 g of the hydrochloride of 1-(4-amino-6,7-dimethoxyquinazolin-2-yl)-4-(3-oxo-5,5-dimethyl-1-cyclohexen-1-yl)-piperazine (78% yield) of melting point 267°-268° C. (decomposition) are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04639453
Source datasetuspto-grants-1987_01
ORD IDord-1e60c489c4ba42d28fff569f6bbcc569
Source noteuspto-grants-1987_01