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HRID 525作成日:2026年10月23日

3-Pyridinemethanamine → 2-N-phenyl-4-N-(pyridin-3-ylmethyl)pyridine-2,4-diamine

https://huagongshe.com/ja/reaction/525

反応式

関与物質

役割名称HCID仕込み量
反応物3-PyridinemethanamineHCID 31018—
反応物4-chloro-N-phenylpyridin-2-amineHCID 23458041—
試薬Sodium t-butoxideHCID 23676156—
触媒(R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t-butylphosphine;Ferrocene, 1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-(dicyclohexylphosphino)-, (2R)-HCID 144543273—
溶媒DimethylacetamideHCID 31374—
生成物2-N-phenyl-4-N-(pyridin-3-ylmethyl)pyridine-2,4-diamineHCID 10188369359.25%

反応条件

温度100 °C

反応手順

Pyridin-3-ylmethanamine (58.1 mg, 0.54 mmol), 4-chloro-N-phenylpyridin-2-amine (100 mg, 0.49 mmol) and sodium 2-methylpropan-2-olate (94 mg, 0.98 mmol) were suspended in DMA (2 mL) and sealed into a microwave tube. Nitrogen was bubbled through the reaction mixture for 5 minutes. (R)-(-)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDI-T-BUTYLPHOSPHINE (32.5 mg, 0.06 mmol) and diacetoxypalladium (8.78 mg, 0.04 mmol) were added to the reaction mixture and nitrogen was bubbled through the reaction mixture for a further 5 minutes. The reaction was heated thermally to 100 °C for 30 mins under nitrogen and cooled to RT. The reaction mixture was neutralised with HCl and purified by ion exchange chromatography, using a 20 g SCX column. The crude product was purified by flash silica chromatography, elution gradient 0 to 10% MeOH in DCM. Fractions containing product were evaporated to dryness to afford N2-phenyl-N4-(pyridin-3-ylmethyl)pyridine-2,4-diamine (80 mg, 59.2 %) as an off white solid.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-4389cfc2af664ae3968b09023440510c
出典メモ750 AstraZeneca ELN dataset