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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791586Generated: November 4, 2026

4-Chloro-6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazoline → HCID 22030614, compound

https://huagongshe.com/reaction/1791586

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazolineHCID 11782230—
Reactant2-Methylquinolin-7-olHCID 135451969—
ProductHCID 22030614HCID 2203061463%

Reaction Steps

Using an analogous procedure to that described in Example 42, 4-chloro-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline (100 mg, 0.31 mmol), (prepared as described for the starting material in Example 10), was reacted with 7-hydroxy-2-methylquinoline (54 mg, 0.34 mmol), (J. Med. Chem. 1998, 41, 4062), to give 6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)-4-(2-methylquinolin-7-yloxy)quinazoline (86 mg, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-2e01c4278d8a4ffc9f7a54bfa168e355
Source noteuspto-grants-2006_07