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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084035Generated: October 31, 2026

4-Chloro-6,7-dimethoxyquinazoline → HCID 22732275, compound

https://huagongshe.com/reaction/2084035

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6,7-dimethoxyquinazolineHCID 2769364—
ReactantN-(3-Aminophenyl)-2-(4-morpholinyl)-4-pyridinecarboxamideHCID 22238130—
ProductHCID 22732275HCID 2273227533%

Reaction Steps

Using an analogous procedure to that described in Example 26, 4-chloro-6,7-dimethoxyquinazoline was reacted with N-(3-aminophenyl)-2-morpholinopyridine-4-carboxamide. The material so obtained was purified by column chromatography eluting with 96:3:1 methylene chloride/methanol/saturated aqueous ammonium hydroxide. The material so obtained was triturated under methylene chloride to give the title compound in 33% yield; NMR: 3.51 (m, 4H), 3.71 (m, 4H), 3.93 (s, 3H), 3.96 (s, 3H), 7.11 (d, 1H), 7.18 (s, 1H), 7.24 (s, 1H), 7.35 (m, 1H), 7.44 (d, 1H), 7.57 (d, 1H), 7.86 (s, 1H), 8.23 (s, 1H), 8.29 (d, 1H), 8.46 (s, 1H), 9.49 (s, 1H), 10.34 (s, 1H); Mass: M+H+ 487.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716847B2
Source datasetuspto-grants-2004_04
ORD IDord-f875100b90cb4fd2989522344a79be3d
Source noteuspto-grants-2004_04