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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454198Generated: November 1, 2026

Ammonium formate → 7-Hydroxy-4-(indol-5-ylamino)-6-methoxyquinazoline

https://huagongshe.com/reaction/454198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant7-Benzyloxy-4(indol-5-ylamino)-6-methoxyquinazoline hydrochlorideHCID 22030547—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product7-Hydroxy-4-(indol-5-ylamino)-6-methoxyquinazolineHCID 13576310697%

Reaction Steps

A solution of give 7-benzyloxy-4-(indol-5-ylamino)-6-methoxyquinazoline hydrochloride (10 g, 23.1 mmol) in methanol (300 ml) and DMF (100 ml) containing ammonium formate (22 gr, 347 mmol) and 10% palladium on charcoal (1 g) was stirred overnight at ambient temperature. The solution was filtered over celite and washed with DMF followed by methanol. The filtrate was evaporated. The residue was dissolved in aqueous ammonia 2 mM (300 ml) and stirred for 15 minutes. The solid was filtered, washed with water followed by ethyl acetate and ether and dried under vacuum at 50° C. for 2 days. The solid was purified by column chromatography eluting with methanol/methylene chloride (1/9). The volatiles were removed under vacuum and the solid was left under vacuum at 70° C. for 2 days to give 7-hydroxy-4-(indol-5-ylamino)-6-methoxyquinazoline (6.8 g, 97%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-cdabee17add045c68e3d937fadb57e56
Source noteuspto-grants-2013_07