Reaktion #742296
ord-2927e481e0ba486fbb770339a97793d5
Reaktionsgleichung
Phosphorus oxychloride
1-(2,6-dichlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ol
→
product
Ausbeute 87.0%
4-chloro-1-(2,6-dichlorophenyl)-1H-pyrazolo[3,4-d]pyrimidine
Ausbeute 87.0%
Reagenzien
Keine
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigereaction
- 2SonstigeThe reaction mixture was evaporated
- 3workup.ADDITIONIce/water and then EtOAc were added
- 4SonstigeThe organic layer to was separated
- 5Extraktionthe aqueous layer re-extracted with EtOAc
- 6WaschenThe combined organics were washed with water
- 7Trocknendried (MgSO4)
- 8Einengenconcentrated
Vorschrift
Phosphorus oxychloride (7.96 mL, 85.38 mmol) was added to 1-(2,6-dichlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ol (Intermediate BA4) (1.2 g, 4.27 mmol). The resulting solution was stiffed at 100° C. for 20 hours. LCMS showed reaction was complete. The reaction mixture was evaporated. Ice/water and then EtOAc were added. The organic layer to was separated and the aqueous layer re-extracted with EtOAc. The combined organics were washed with water, dried (MgSO4) and concentrated to give the product (1.110 g, 87%) which was used without further purification. 1H NMR (400 MHz, CDCl3) δ 7.46-7.58 (3H, m), 8.45 (1H, s), 8.82 (1H, s); m/z (ES+) (M+H)+=299; HPLC tR=2.77 min.