Reacción #8681
ord-b7adf5f83e484202bbbfe8a0c301bb8c
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
110°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1workup.ADDITIONpoured
- 2workup.DISTILLATIONinto distilled water
- 3FiltraciónThe precipitated solid is filtered off
- 4Lavadowashed with distilled water
- 5Otrodried
- 6Otro93 mg (64% of theory) of the product are obtained
- 7Otroare directly reacted further without further purification
Procedimiento
100 mg (0.26 mmol) of 1-cyclopropyl-2-{2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]-pyridin-3-yl]-5-pyrimidinyl}ethanone (example XXVI, step 1) are added to a solution of 123 mg (1.03 mmol) of N-(dimethoxymethyl)-N,N-dimethylamine in 1 ml of DMF. The reaction mixture is stirred at 110° C. for 2 hours and then poured into distilled water. The precipitated solid is filtered off, washed with distilled water and dried. 93 mg (64% of theory) of the product are obtained and are directly reacted further without further purification.