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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454281Generated: October 30, 2026

1-(3-Aminopropyl)-4-methylpiperazine → HCID 54524703, compound

https://huagongshe.com/reaction/454281

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Aminopropyl)-4-methylpiperazineHCID 78328—
Reactant(2R)-6-methoxy-4-(3-methylindol-5-yloxy)-7-(oxiran-2-ylmethoxy)quinazolineHCID 54069082—
SolventDimethylformamideHCID 6228—
ProductHCID 54524703HCID 5452470331%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of (2R)-6-methoxy-4-(3-methylindol-5-yloxy)-7-(oxiran-2-ylmethoxy)quinazoline (100 mg, 0.28 mmol), (prepared as described in Example 278), and 1-(3-aminopropyl)-4-methylpiperazine (132 mg, 0.84 mmol) in DMF (5 ml) was heated to 70° C. for 3 hours. The solvents were removed in vacuo and the residue taken up in dichloromethane. This was washed with water, dried (MgSO4), filtered and evaporated. The residue was purified by silica column chromatography using gradient elution (dichloromethane, 5% methanol/95% dichloromethane, 20% methanolic ammonia (7M)/80% dichloromethane) to give (2R)-7-(2-hydroxy-3-(3-(4-methylpiperazin-1-yl)propylamino)propoxy)-6-methoxy-4-(3-methylindol-5-yloxy)quinazoline (44 mg, 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-9a592a97bdba4ae0b35de335e8918164
Source noteuspto-grants-2013_07