Reacción #674353

ord-a7c9b58ff01c49a29a88edf8c0be760c

Ecuación de reacción

NS(=O)(=O)Cc1cccc(Nc2ncnc(Cl)n2)c1
A1
NS(=O)(=O)Cc1cccc(Nc2ncnc(Cl)n2)c1
3-[(4-Chloro-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamide
Cl.c1ncc2c(n1)CCNC2
5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine hydrochloride
→
NS(=O)(=O)Cc1cccc(Nc2ncnc(N3CCc4ncncc4C3)n2)c1
3-[(4-(7,8-Dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamide

Reactantes

NS(=O)(=O)Cc1cccc(Nc2ncnc(Cl)n2)c1
A1
NS(=O)(=O)Cc1cccc(Nc2ncnc(Cl)n2)c1
3-[(4-Chloro-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamide
Cl.c1ncc2c(n1)CCNC2
5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine hydrochloride

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroB39 was prepared

Procedimiento

B39 was prepared following the general procedure reported for B10 using A1 and 5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine hydrochloride; yield: 29.7 mg (7%), pale yellow solid. MS (ES) C17H18N8O2S requires: 398. found: 399 (M+H)+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09226929B2uspto-grants-2016_01