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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454081Generated: October 30, 2026

HCID 22030925, compound → HCID 22030827, compound

https://huagongshe.com/reaction/454081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22030925HCID 22030925—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventAcrylonitrileHCID 7855—
ProductHCID 22030827HCID 22030827171.2%

Reaction Steps

A solution of 6-methoxy-4-(2-methylindol-5-yloxy)-7-(2-(piperidin-4-yloxy)ethoxy)quinazoline (76 mg, 0.17 mmol), (prepared as described in Example 77), in acrylonitrile (0.5 ml), methylene chloride (1 ml) and methanol (1 ml) was stirred overnight at ambient temperature. After removal of the volatiles under vacuum the residue was purified by column chromatography eluting with methylene chloride/methanol (98/2 followed by 95/5 and 90/10). The residue was triturated with ethyl acetate and ether. The resulting solid was filtered and dried under vacuum to give 7-(2-(1-(2-cyanoethyl)piperidin-4-yloxy)ethoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline (73 mg, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-abe1941879dd4d25a3deb7b174921283
Source noteuspto-grants-2013_07