Reaction #674354

ord-5277f88441c740dca69396dbf97d0261

Reaction equation

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
c1ccc2c(c1)CCNC2
1,2,3,4-tetrahydroisoquinoline
→
NS(=O)(=O)Cc1cccc(Nc2ncnc(N3CCc4ccccc4C3)n2)c1
3-[(4-(3,4-Dihydroisoquinolin-2(1H)-yl)-1,3,5-triazin-2-yl)amino]-benzenemethanesulfonamide

Reactants

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
c1ccc2c(c1)CCNC2
1,2,3,4-tetrahydroisoquinoline

Reagents

None

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherB40 was prepared

Procedure

B40 was prepared following the general procedure reported for B10 using A1 and 1,2,3,4-tetrahydroisoquinoline; yield: 23.6 mg (6%), colorless amorphous solid. MS (ES) C19H20N6O2S requires: 396. found: 397 (M+H)+.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09226929B2uspto-grants-2016_01