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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454075Generated: October 29, 2026

Tetrahydrofuran → 7-(2-Carboxyvinyl)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline

https://huagongshe.com/reaction/454075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-methyl-1H-indol-5-olHCID 83336—
ReactantSodium hexamethyidisilazaneHCID 45051731—
Reactant7-(2-Carboxyvinyl)-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazolineHCID 54194426—
SolventDimethyl SulfoxideHCID 679—
Product7-(2-Carboxyvinyl)-6-methoxy-4-(2-methylindol-5-yloxy)quinazolineHCID 5443345571.4%

Reaction Steps

1M Sodium HMDS in THF (0.84 ml, 8.4 mmol) was added to a suspension of 7-(2-carboxyvinyl)-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazoline (105 mg, 0.28 mmol) and 5-hydroxy-2-methylindole (82 mg, 0.56 mmol), (prepared as described for the starting material in Example 48), in DMSO (1.5 ml). After stirring for 2 hours at ambient temperature, the mixture was partitioned between ethyl acetate and water. The aqueous layer was adjusted to pH3 with 2M hydrochloric acid. The organic layer was washed with water, brine, dried (MgSO4) and evaporated. The residue was purified by column chromatography eluting with methylene chloride/methanol (95/5 followed by 90/10 and 70/30) to give 7-(2-carboxyvinyl)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline (75 mg, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-87f11fb55b1b4e1c902cd7d96f703733
Source noteuspto-grants-2013_07