Réaction #44681

Équation de réaction

hydrochloric acid

4-amino-1H-pyrrolo[2,3-b]pyridine

4-Amino-1H-pyrrolo[2,3-b]pyridine

isopentyl nitrite

→

4-Chloro-1H-pyrrolo[2,3-b]pyridine

Solvants

acetic acid

sulfuric acid

Conditions de réaction

Traitement

1. 1
   Températurethe mixture is then heated at 80-90° C. for 30 min
2. 2
   TempératureThe mixture is cooled to RT
3. 3
   workup.STIRRINGstirred overnight
4. 4
   ConcentrationFor work-up, the reaction solution is concentrated
5. 5
   Filtrationthe precipitated copper salts are filtered off with suction through kieselguhr
6. 6
   Extractionthe mixture is extracted 3× with ethyl acetate
7. 7
   SéchageThe organic phase is dried over magnesium sulfate
8. 8
   Concentrationconcentrated
9. 9
   Autrea rotary evaporator

Mode opératoire

750 mg (5.63 mmol) of 4-amino-1H-pyrrolo[2,3-b]pyridine (from example XVII) are dissolved in a mixture of 67.5 ml of glacial acetic acid and 0.67 ml of concentrated sulfuric acid. The mixture is cooled to 12° C. 3.67 ml (3.20 g, 117 mmol) of isopentyl nitrite are slowly added dropwise, and the mixture is stirred at 12° C. for 3 hours. This solution is then added to a suspension (temperature: 50° C.) of 6.07 g (61.4 mmol) of copper(I) chloride in 34 ml of concentrated hydrochloric acid, and the mixture is then heated at 80-90° C. for 30 min. The mixture is cooled to RT and stirred overnight. For work-up, the reaction solution is concentrated and made alkaline using 1N aqueous sodium hydroxide solution, the precipitated copper salts are filtered off with suction through kieselguhr and the mixture is extracted 3× with ethyl acetate. The organic phase is dried over magnesium sulfate and concentrated using a rotary evaporator.

Source