تفاعل #690

ord-7d0087e63ad44356ba79974b84233090

معادلة التفاعل

Clc1ccnc(Nc2ccccc2)c1
Clc1ccnc(Nc2ccccc2)c
NCc1c(F)cccc1F
NCc1c(F)cccc1F
Fc1cccc(F)c1CNc1ccnc(Nc2ccccc2)c1
Fc1cccc(F)c1CNc1ccnc
المردود 21.0%

المذيبات

ظروف التفاعل

درجة الحرارة
150°CELSIUS

الإجراء التجريبي

4-chloro-N-phenylpyridin-2-amine (100 mg, 0.49 mmol), (2,6-difluorophenyl)methanamine (91 mg, 0.64 mmol), (R)-(-)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDI-T-BUTYLPHOSPHINE (32.5 mg, 0.06 mmol),sodium 2-methylpropan-2-olate (94 mg, 0.98 mmol) and diacetoxypalladium (8.78 mg, 0.04 mmol) were suspended in DME (2.0 mL) and sealed into a microwave tube. The reaction was heated to 150 °C for 20 minutes in the microwave reactor and cooled to RT. The crude product was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH and fractions were evaporated to dryness to afford crude product. The crude product was purified by preparative HPLC (Waters XBridge Prep C18 OBD column, 5µ silica, 50 mm diameter, 100 mm length), using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford N4-(2,6-difluorobenzyl)-N2-phenylpyridine-2,4-diamine (32.0 mg, 21.04 %) as a yellow gum.

المصدر

750 AstraZeneca ELN dataset