Reaction #674355

ord-a7fd5636d61e48be8ed04ea6bc4f4495

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
Nc1cccc2c1CCNC2
5-amino-1,2,3,4-tetrahydroisoquinoline
→
Nc1cccc2c1CCN(c1ncnc(Nc3cccc(CS(N)(=O)=O)c3)n1)C2
3-[(4-(5-Amino-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
Nc1cccc2c1CCNC2
5-amino-1,2,3,4-tetrahydroisoquinoline

Reagents

None

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherB41 was prepared

Procedure

B41 was prepared following the general procedure reported for B10 using A1 and 5-amino-1,2,3,4-tetrahydroisoquinoline; yield: 61.5 mg (15%), pale yellow solid. MS (ES) C19H21N7O2S requires: 411. found: 412 (M+H)+.

Source

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