HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354814Generated: October 30, 2026
Isoamyl Alcohol → HCID 13100541, compound
https://huagongshe.com/reaction/354814
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoamyl Alcohol | HCID 31260 | — |
| Reactant | 1-(Tetrahydro-2-furoyl)piperazine | HCID 2734641 | — |
| Reactant | HCID 12920006 | HCID 12920006 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13100541 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04377581 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-0238c0dc2813490597e1c831bdf81d3a |
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| Source note | uspto-grants-1983_03 |
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