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HRID 269作成日:2026年10月23日

3-methoxy-4-(4-methyl-1H-imidazol-1-yl)aniline → (R)-N-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-6-methyl-8-phenyl-5,6,7,8-tetrahydropyrimido[5,4-f][1,4]oxazepin-2-amine

https://huagongshe.com/ja/reaction/269

反応式

関与物質

役割名称HCID仕込み量
反応物3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 45480181—
反応物(R)-2-chloro-6-methyl-8-phenyl-5,6,7,8-tetrahydropyrimido[5,4-f][1,4]oxazepineHCID 59577867—
試薬Cesium carbonateHCID 10796—
触媒Tris(1,1-dimethylethyl)phosphineHCID 83681—
触媒Palladium (II) acetateHCID 4144353—
溶媒1,4-DioxaneHCID 31275—
生成物(R)-N-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-6-methyl-8-phenyl-5,6,7,8-tetrahydropyrimido[5,4-f][1,4]oxazepin-2-amineHCID 4982085915%

反応条件

温度120 °C

反応手順

(R)-2-chloro-6-methyl-8-phenyl-5,6,7,8-tetrahydropyrimido[5,4-f][1,4]oxazepine (0.05 g, 0.18 mmol), 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)aniline (0.037 g, 0.18 mmol) (0.65), PALLADIUM(II) ACETATE (1.221 mg, 5.44 µmol), CESIUM CARBONATE (0.071 g, 0.22 mmol) and Tri-tert- butylphosphonium tetrafluoriborate (0.0043 g, 0.014 mmol, 6 mol%) in 1 ml of dioxane was degaset over argone and heated in MW 120°C 30 min. 002 - 4.8% of conversion mixture was heated more in MW 140°C 30 min. 003 - 15% of conversion mixture was heated more in MW 160°C 30 min. Experiment was not progressed.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-3d675e76027a44c193655dafbce49365
出典メモ750 AstraZeneca ELN dataset