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HRID 2361046作成日:2026年10月27日

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

https://huagongshe.com/reaction/2361046

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)pyridin-4-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US08686155B2
出典データセットuspto-grants-2014_04
ORD IDord-e396a48e028243ec828c936e5857f4be
出典メモuspto-grants-2014_04