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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464286Generated: October 30, 2026

Diisopropyl Ether → 1-[4-{4-(2-Aminophenyl)piperazin-1-yl)butyl]-2,4(1H,3H)-quinazolinedione

https://huagongshe.com/reaction/1464286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl EtherHCID 7914—
ReactantStannous ChlorideHCID 24479—
ReactantHCID 19087663HCID 19087663—
SolventEthanolHCID 702—
Product1-[4-{4-(2-Aminophenyl)piperazin-1-yl)butyl]-2,4(1H,3H)-quinazolinedioneHCID 1908768437.1%

Reaction Steps

To a solution of 1-[4-{4-(2-nitrophenyl)piperazin-1-yl}butyl]-2,4(1H,3H)-quinazolinedione (90 mg) in ethanol (8 ml) was added tin(II) chloride (159 mg) at 80° C. After stirring for 1 hour at the same temperature, the reaction mixture was quenched with ice and saturated aqueous sodium bicarbonate, and extracted with chloroform. The organic extract was washed with saturated aqueous sodium bicarbonate, dried over magnesium sulfate, and evaporated to give an amorphous. 1-[4-{4-(2-Aminophenyl)piperazin-1-yl)butyl]-2,4(1H,3H)-quinazolinedione (31 mg) was obtained by crystallization of the amorphous from diisopropyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05304560
Source datasetuspto-grants-1994_04
ORD IDord-28be445cd86d4458a8b7497459957913
Source noteuspto-grants-1994_04