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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791565Generated: November 3, 2026

6-Hydroxy-2H-1,4-benzoxazin-3(4H)-one → 6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)-4-(3-oxo-2H-4H-1,4-benzoxazin-6-yloxy)quinazoline

https://huagongshe.com/reaction/1791565

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Hydroxy-2H-1,4-benzoxazin-3(4H)-oneHCID 11378689—
Reactant4-Chloro-6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazolineHCID 11782230—
Product6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)-4-(3-oxo-2H-4H-1,4-benzoxazin-6-yloxy)quinazolineHCID 2203057988%

Reaction Steps

Using a procedure analogous to that described for Example 9, 4-chloro-6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazoline (0.13 g, 0.4 mmol), (prepared as described for the starting material in Example 10), was reacted with 6-hydroxy-2H-4H-1,4-benzoxazin-3-one (83 mg, 0.5 mmol), (J. Chem. Soc. C, 1971, 2696), to give 6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)-4-(3-oxo-2H-4H-1,4-benzoxazin-6-yloxy)quinazoline (158 mg, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-5a514b9975c547d895e0fc229b7da49d
Source noteuspto-grants-2006_07