反応 #90811

ord-54da0cd2dccb47709c1b181e15a3543d

反応方程式

Clc1cc(I)c(Cl)cn1
2,5-dichloro-4-iodopyridine
N#Cc1cc(Cl)ccc1N
2-amino-5-chlorobenzonitrile
O=P([O-])([O-])OP(=O)([O-])OP(=O)([O-])[O-].[K+].[K+].[K+].[K+].[K+]
potassium triphosphate
c1ccc(P(c2ccccc2)c2ccccc2Oc2ccccc2P(c2ccccc2)c2ccccc2)cc1
DPEPhos
N#Cc1cc(Cl)ccc1Nc1cc(Cl)ncc1Cl
5-chloro-2-[(2,5-dichloro-4-pyridinyl)amino]benzonitrile
収率 33.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度at reflux for 18 hr
  2. 2
    ろ過The reaction mixture was filtered
  3. 3
    その他The reaction mixture was evaporated
  4. 4
    workup.ADDITIONEther (50 ml) was added
  5. 5
    ろ過the solid was filtered

実験手順

To a degassed solution of 2,5-dichloro-4-iodopyridine (4.5 g, 16.43 mmol), 2-amino-5-chlorobenzonitrile (2.507 g, 16.43 mmol) and potassium triphosphate (10.46 g, 49.3 mmol) in 1,4-dioxane (60 ml) stirred under nitrogen at the room temperature was added DPEPhos (0.708 g, 1.314 mmol) and palladium acetate (0.148 g, 0.657 mmol). The reaction mixture was stirred at reflux for 18 hr. The reaction mixture was filtered. The reaction mixture was evaporated. Ether (50 ml) was added and the solid was filtered. 5-chloro-2-[(2,5-dichloro-4-pyridinyl)amino]benzonitrile (1.8 g, 5.43 mmol, 33.0% yield) was isolated as orange solid. 1H NMR (400 MHz, DMSO-d6) ppm 6.63 (s, 1 H) 7.52 (d, J=8.59 Hz, 1 H) 7.81 (dd, J=8.59, 2.53 Hz, 1 H) 8.09 (d, J=2.53 Hz, 1 H) 8.24 (s, 1 H) 9.06 (br. s., 1 H); HPLC Rt=3.53 min, MS (ESI): 298.0, 299.9 [M+H]+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09446034B2uspto-grants-2016_09