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HRID 537作成日:2026年10月26日

Benzylamine → 4-N-benzyl-2-N-phenylpyridine-2,4-diamine

https://huagongshe.com/reaction/537

反応式

関与物質

役割名称HCID仕込み量
反応物BenzylamineHCID 7504—
反応物4-chloro-N-phenylpyridin-2-amineHCID 23458041—
試薬Sodium t-butoxideHCID 23676156—
触媒Palladium (II) acetateHCID 4144353—
触媒2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
溶媒DimethylacetamideHCID 31374—
生成物4-N-benzyl-2-N-phenylpyridine-2,4-diamineHCID 10188368813.23%

反応条件

温度100 °C

反応手順

Phenylmethanamine (57.6 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. 2-Dicyclohexylphosphino-2',6'-di- i-propoxy-1,1'-biphenyl (27.4 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 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 preparative HPLC (Waters SunFire column, 5µ silica, 50 mm diameter, 100 mm length), using decreasingly polar mixtures of water (containing 0.1% formic acid) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness N4-benzyl-N2-phenylpyridine-2,4-diamine (17.80 mg, 13.23 %) 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-6ec08990002f44da89217320c1b9e8f7
出典メモ750 AstraZeneca ELN dataset