Reacción #68943

Ecuación de reacción

3-chloroisoquinoline

5-amino-3-(1-(dimethylamino)propan-2-yloxy)pyrazine-2-carbonitrile

sodium tert-butoxide

TsOH

→

title compound

Rendimiento 7.2%

3-(1-(Dimethylamino)propan-2-yloxy)-5-(isoquinolin-3-ylamino)pyrazine-2-carbonitrile

Rendimiento 7.2%

Disolventes

DMF

toluene

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrowas degassed under a stream of nitrogen gas
2. 2
   Otrothe mixture was degassed for a further 5 minutes
3. 3
   TemperaturaUpon cooling
4. 4
   workup.ADDITIONthe mixture was diluted with methanol
5. 5
   Otroisolated by SPE
6. 6
   Lavadowashing with methanol
7. 7
   Lavadoeluting with 2 M ammonia in methanol
8. 8
   Concentraciónconcentrated in vacuo

Procedimiento

A mixture of palladium (II) acetate (24 mg, 0.11 mmol) and (±)-2,2″-bis(diphenylphosphino)-1,1″-binaphthalene (140 mg, 0.22 mmol) in toluene (2 mL) was degassed under a stream of nitrogen gas with stirring for 10 minutes. After addition of 3-chloroisoquinoline (59 mg, 0.36 mmol), 5-amino-3-(1-(dimethylamino)propan-2-yloxy)pyrazine-2-carbonitrile (80 mg, 0.36 mmol) in DMF (0.5 mL), and sodium tert-butoxide (42 mg, 0.43 mmol), the mixture was degassed for a further 5 minutes and then heated at 140° C. for 30 minutes in a microwave reactor. Upon cooling, the mixture was diluted with methanol and isolated by SPE using a MP-TsOH cartridge, washing with methanol and then eluting with 2 M ammonia in methanol. The basic fractions were combined and concentrated in vacuo. Preparative HPLC gave the title compound (8.9 mg, 0.026 mmol, 7%). 1H NMR (d6-DMSO, 400 MHz) δ 9.22 (s, 1H), 8.45 (s, 1H), 8.23 (s, 1H), 8.09 (d, 1H, J=9.1 Hz), 7.84 (d, 1H, J=8.1 Hz), 7.77-7.73 (m, 1H), 7.58-7.54 (m, 1H), 5.53-5.49 (m, 1H), 2.67-2.63 (m, 1H), 2.34-2.32 (m, 1H), 2.21 (s, 6H), 1.46 (d, 3H, J=6.3 Hz). LC-MS (2) Rt=2.93 min m/z (ESI−) 347 (M−H).

Fuente