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HRID 279556作成日:2026年10月26日

Acetic Acid → 4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-(2-(imidazol-1-yl)ethoxy)-6-methoxyquinazoline

https://huagongshe.com/reaction/279556

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物TriphenylphosphineHCID 11776—
反応物N-(2-Hydroxyethyl)imidazoleHCID 74168—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline hydrochlorideHCID 135671179—
溶媒DichloromethaneHCID 6344—
生成物4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-(2-(imidazol-1-yl)ethoxy)-6-methoxyquinazolineHCID 2262502576.4%

反応手順

Diethyl azodicarboxylate (160 mg, 1.4 mmol) was added to a solution of 4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline hydrochloride (261 mg, 0.7 mmol), (prepared as described for the starting material in Example 22), triphenylphosphine (367 mg, 1.4 mmol) and 2-(imidazol-1-yl)ethanol (94 mg, 0.84 mmol), (J. Med. Chem. 1993, 25, 4052-4060), in methylene chloride (5 ml) and the mixture stirred for 1 hour at ambient temperature. Acetic acid (42 mg, 0.7 mmol) was added and the solvent was removed by evaporation. The residue was triturated with ether, the solid collected by filtration, dried under vacuum and purified by chromatography eluting with methylene chloride/methanol (9/1 followed by 8/2) to give 4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-(2-(imidazol-1-yl)ethoxy)-6-methoxyquinazoline (250 mg, 76%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06362336B1
出典データセットuspto-grants-2002_03
ORD IDord-b09be4b4f04f4c91b265718ae24c509e
出典メモuspto-grants-2002_03