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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357708Generated: October 24, 2026

HCID 17904941, compound → 6-Acetoxy-7-methoxy-4-[2-methyl-5-(2-morpholinopyridine-4-carboxamido)anilino]quinazoline Dihydrochloride

https://huagongshe.com/reaction/1357708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 17904941HCID 17904941—
Reactant4-Chloro-7-methoxyquinazolin-6-yl acetate--hydrogen chloride (1/1)HCID 22022159—
SolventIsopropanolHCID 3776—
Product6-Acetoxy-7-methoxy-4-[2-methyl-5-(2-morpholinopyridine-4-carboxamido)anilino]quinazoline DihydrochlorideHCID 2273224780%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of N-(3-amino-4-methylphenyl)-2-morpholinopyridine-4-carboxamide (178 mg), 6-acetoxy-4-chloro-7-methoxyquinazoline hydrochloride (150 mg) and isopropanol (5 ml) was stirred and heated to 85° C. for 3 hours. The reaction mixture was allowed to cool to ambient temperature and the solid was isolated and washed in turn with isopropanol (5 ml) and isohexane (2×5 ml). There was thus obtained the title compound (249 mg, 80%); NMR: 2.17 (s, 3H), 2.38 (s, 3H), 3.56 (m, 4H), 3.72 (m, 4H), 4.0 (s, 3H), 7.16 (m, 1H), 7.37 (m, 2H), 7.52 (s, 1H), 7.68 (m, 1H), 7.87 (m, 1H), 8.24 (m, 1H), 8.67 (s, 1H), 8.8 (s, 1H), 10.6 (s, 1H), 11.50 (s, 1H); m/s: M+H+ 529.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593333B1
Source datasetuspto-grants-2003_07
ORD IDord-e3fbb0c15761475b9c44c4750f971983
Source noteuspto-grants-2003_07