聚(苯乙烯-二乙烯苯) → 4-N-benzyl-2-N-phenylpyridine-2,4-diamine

HRID 538

反应方程式

HRID 538 反应方程式
Clc1ccnc(Nc2ccccc2)c1.NCc1ccccc1>CC(=O)N(C)C.CC(=O)O.CC(=O)O.CC(C)(C)[O-].COc1ccc(OC)c(P(C2CCCCC2)C2CCCCC2)c1-c1c(C(C)C)cc(C(C)C)cc1C(C)C.[Na+].[Pd]>c1ccc(CNc2ccnc(Nc3ccccc3)c2)cc1

参与物

7

反应条件

温度
100 °C

实验过程

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. Dicyclohexyl(2',4',6'-triisopropyl-3,6-dimethoxy-[1,1'-biphenyl]-2-yl)phosphine (31.5 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 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 product were evaporated to dryness to afford N4-benzyl-N2-phenylpyridine-2,4-diamine (8.50 mg, 6.32 %) as an off white solid.

来源与证据

ORD记录
ord-34a984f4da874bc6bcf03a1eda073eec
来源数据集
750 AstraZeneca ELN dataset
原始链接
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