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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241580Generated: October 30, 2026

4-Chloro-6-methoxy-7-(3-(4-methylpiperazin-1-yl)propoxy)quinazoline → HCID 21936057, compound

https://huagongshe.com/reaction/1241580

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6-methoxy-7-(3-(4-methylpiperazin-1-yl)propoxy)quinazolineHCID 11245061—
Reactant5-Bromo-2H-1,3-benzodioxol-4-amineHCID 21936013—
ProductHCID 21936057HCID 21936057—

Reaction Steps

Using an analogous procedure to that described in Example 15, 4-chloro-6-methoxy-7-[3-(4-methylpiperazin-1-yl)propoxy]quinazoline was reacted with 6-bromo-2,3-Methylenedioxyaniline to give the title compound as a solid; NMR Spectrum: DMSOd6 and CF3CO2D) 2.3 (m, 2H), 2.95 (s, 3H), 3.2–3.9 (br s, 8H), 3.4 (m, 2H), 4.0 (s, 3H), 4.35 (m, 2H), 6.15 (s, 2H), 7.05 (d, 1H), 7.3 (d, 1H), 7.4 (s, 1H), 8.15 (s, 1H), 8.9 (s, 1H); Mass Spectrum: M+H+ 530 and 532; Elemental Analysis: Found C, 54.25; H, 5.54; N, 12.8. C24H28BrN5O4 requires C, 54.35; H, 5.32; N, 13.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115615B2
Source datasetuspto-grants-2006_10
ORD IDord-facc6c9564654b8c9fe2828aac488eee
Source noteuspto-grants-2006_10