Reacción #487565

ord-e498f861ae174ada895725af89f3a418

Ecuación de reacción

[Na+].[OH-]
NaOH
[O-][n+]1cccc2cc[nH]c21
1H-pyrrolo[2,3-b]pyridine 7-oxide
CN(C)C=O
N,N-dimethylformamide
CS(=O)(=O)Cl
methanesulfonyl chloride
Clc1ccnc2[nH]ccc12
wet pale orange solid
Rendimiento 135.4%
Clc1ccnc2[nH]ccc12
4-Chloro-1H-pyrrolo[2,3-b]pyridine
Rendimiento 135.4%

Disolventes

Condiciones de reacción

Temperatura
73°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled to 40° C
  2. 2
    Temperaturathe resulting suspension was cooled to 0° C
  3. 3
    FiltraciónThe mixture was filtered
  4. 4
    Lavadowashed with water (×3)

Procedimiento

To a 50° C. pink solution of 1H-pyrrolo[2,3-b]pyridine 7-oxide (2.47 g, 0.0184 mol) in N,N-dimethylformamide (13.3 mL, 0.172 mol) was added methanesulfonyl chloride (4.0 mL, 0.052 mol). The pink color changed to orange. The mixture was heated to 73° C. for 2 h, and cooled to 40° C. Then 35 mL of water was added and the resulting suspension was cooled to 0° C. NaOH was added to adjust the pH of the mixture to ˜7. The mixture was filtered and washed with water (×3) to give 3.8 g of wet pale orange solid that was dried at 40° C. overnight to give 2.35 g (82.2% yield).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08741895B2uspto-grants-2014_06