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HRID 227779作成日:2026年10月24日

tert-Butanol → N-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenylphthalazin-1-amine

https://huagongshe.com/ja/reaction/227779

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物1-Chloro-4-phenylphthalazineHCID 272109—
反応物4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyridin-2-amineHCID 66735161—
溶媒Diethyl EtherHCID 3283—
溶媒Sodium CarbonateHCID 10340—
生成物N-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenylphthalazin-1-amineHCID 57756271—

反応条件

温度100 °C

反応手順

To 4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyridin-2-amine (0.070 g, 0.24 mmol) and 1-chloro-4-phenylphthalazine (0.048 g, 0.20 mmol) was added tBuOH (1.0 mL). The resulting mixture was heated at 100° C. in a sealed tube for 16 hours. The reaction was diluted with diethyl ether and saturated sodium carbonate and vigorously shaken. The resulting solids were filtered and washed with water, diethyl ether and air dried to yield N-(4-(3-(2-(methylamino)pyridin4-yl)pyridin-2-yloxy)phenyl)-4-phenylphthalazin-1-amine as an off-white solid. MS m/z=497 [M+H]+. Calc'd for C31H24N6O: 496.58.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560551B2
出典データセットuspto-grants-2009_07
ORD IDord-11513d24343d495cade845c8575d7159
出典メモuspto-grants-2009_07