تفاعل #641

ord-edb6c9cf54a940259581c192883091b5

معادلة التفاعل

Clc1ccnc(Nc2ccccc2)c1
Clc1ccnc(Nc2ccccc2)c
NCc1ccccc1
NCc1ccccc1
c1ccc(CNc2ccnc(Nc3ccccc3)c2)cc1
c1ccc(CNc2ccnc(Nc3cc
المردود 69.1%

المذيبات

ظروف التفاعل

درجة الحرارة
100°CELSIUS

الإجراء التجريبي

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. (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 in DMA (1 mL). 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 N4-benzyl-N2-phenylpyridine-2,4-diamine (93 mg, 69.1 %) as an off-white solid.

المصدر

750 AstraZeneca ELN dataset