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HRID 2084017作成日:2026年10月26日

N-(3-amino-4-methylphenyl)-2-morpholinopyridine-4-carboxamide → 6-Acetoxy-7-methoxy-4-[2-methyl-5-(2-morpholinopyridine-4-carboxamido)anilino]quinazoline Dihydrochloride

https://huagongshe.com/reaction/2084017

反応式

関与物質

役割名称HCID仕込み量
反応物N-(3-amino-4-methylphenyl)-2-morpholinopyridine-4-carboxamideHCID 17904941—
反応物4-Chloro-7-methoxyquinazolin-6-yl acetate--hydrogen chloride (1/1)HCID 22022159—
溶媒IsopropanolHCID 3776—
生成物6-Acetoxy-7-methoxy-4-[2-methyl-5-(2-morpholinopyridine-4-carboxamido)anilino]quinazoline DihydrochlorideHCID 2273224780%

反応条件

温度85 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06716847B2
出典データセットuspto-grants-2004_04
ORD IDord-4ebd3b192c98400c8213269fb995b7d1
出典メモuspto-grants-2004_04