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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354814Generated: October 30, 2026

Isoamyl Alcohol → HCID 13100541, compound

https://huagongshe.com/reaction/354814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl AlcoholHCID 31260—
Reactant1-(Tetrahydro-2-furoyl)piperazineHCID 2734641—
ReactantHCID 12920006HCID 12920006—
SolventDiethyl EtherHCID 3283—
ProductHCID 13100541HCID 13100541—

Reaction Steps

To 35 ml. of isoamyl alcohol were added 1.50 g. (5.47 mmole) of 4-amino-2,6-dichloro-7,8-dimethoxyquinazoline and 1.11 g. (6.02 mmole) of 1-(2-tetrahydrofuroyl)piperazine and the mixture was heated at reflux under a nitrogen atmosphere for 1.5 hours. The mixture was cooled, 20 ml. of ethyl ether was added and the resulting mixture stirred at room temperature overnight. It was then cooled in ice and the precipitated solid collected by filtration. The crude material was recrystallized once from a mixture of isopropanol, methanol and ethyl ether. The recrystallized material was dissolved in water made strongly alkaline with sodium hydroxide solution while stirring, the precipitated brownish solid collected by filtration, dried, decolorized with activated carbon and recrystallized from isopropanol/ethyl ether to obtain 0.38 g. of yellow solid, M.P. 192°-193° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04377581
Source datasetuspto-grants-1983_03
ORD IDord-0238c0dc2813490597e1c831bdf81d3a
Source noteuspto-grants-1983_03