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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791669Generated: November 3, 2026

1-Methylpiperazine → HCID 22030739, compound

https://huagongshe.com/reaction/1791669

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 22030772HCID 22030772—
SolventDimethylformamideHCID 6228—
ProductHCID 22030739HCID 2203073932%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 7-(2,3-epoxypropoxy)-6-methoxy-4-(2-methylindol-5-yloxy) quinazoline (100 mg, 0.27 mmol), (prepared as described for the starting material in Example 162), and N-methylpiperazine (200 ul, 1.8 mmol) in DMF (4 ml) was heated at 70° C. for 24 hours. The solvent was removed by evaporation and the residue was recrystallised from acetonitrile. The solid was filtered, washed with diethyl ether and dried to give 7-(2-hydroxy-3-(4-methylpiperazin-1-yl)propoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline (41 mg, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-df2ac05840054c5486acbdaca480a418
Source noteuspto-grants-2006_07