反応 #633

ord-6ec08990002f44da89217320c1b9e8f7

反応方程式

Clc1ccnc(Nc2ccccc2)c1
Clc1ccnc(Nc2ccccc2)c
NCc1ccccc1
NCc1ccccc1
c1ccc(CNc2ccnc(Nc3ccccc3)c2)cc1
c1ccc(CNc2ccnc(Nc3cc
収率 13.2%

反応条件

温度
100°CELSIUS

実験手順

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.

出典

750 AstraZeneca ELN dataset