Réaction #674327

ord-b4f11277db614da5836265594a9815c6

Équation de réaction

NS(=O)(=O)Cc1cccc(Nc2ncnc(Cl)n2)c1
triazine
NS(=O)(=O)Cc1cccc(Nc2ncnc(Cl)n2)c1
3-[(4-Chloro-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamide
C1COCCN1
morpholine
CCN(C(C)C)C(C)C
DIPEA
NS(=O)(=O)Cc1cccc(Nc2ncnc(N3CCOCC3)n2)c1
3-[(4-(Morpholin-4-yl)-1,3,5-triazin-2-yl)amino]benzenemethane sulfonamide

Solvants

Conditions de réaction

Température
60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe solvent removed under reduced pressure
  2. 2
    workup.ADDITIONThe residue was treated with MeOH
  3. 3
    Filtrationthe solid title compound (B10) collected by filtration
  4. 4
    Lavagewashed with MeOH
  5. 5
    Autredried in vacuo

Mode opératoire

To a solution of triazine A1 (300 mg, 1.0 mmol) in a mixture of THF (4 mL) and iPrOH (4 mL) were added morpholine (87 mg, 1.0 mmol) and DIPEA (200 μL, 1.15 mmol). The mixture was heated for 2 hours at 60° C. and the solvent removed under reduced pressure. The residue was treated with MeOH and the solid title compound (B10) collected by filtration, washed with MeOH, and dried in vacuo. Yield: 93.3 mg (27%), colorless amorphous solid. MS (ES) C14H18N6O3S requires: 350. found: 351 (M+H)+.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09226929B2uspto-grants-2016_01