Réaction #487541

ord-71fd19f5bc3d4f2db17b3f9229728784

Équation de réaction

CC(C)OC(=O)/N=N/C(=O)OC(C)C
DIAD
COC(=O)c1ccc(Nc2nc(Cl)nc(OCC(F)(F)F)n2)cc1O
methyl 4-(4-chloro-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)-2-hydroxybenzoate
CC(C)(C)OC(=O)NCCCCCCO
tert-butyl 6-hydroxyhexylcarbamate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
Triphenylphosphine
COC(=O)c1ccc(Nc2nc(Cl)nc(OCC(F)(F)F)n2)cc1OCCCCCCNC(=O)OC(C)(C)C
methyl 2-(6-(tert-butoxycarbonylamino)hexyloxy)-4-(4-chloro-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzoate
Rendement 36.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe solvent was removed under vacuum
  2. 2
    Autrethe crude product was purified by silica gel chromatography
  3. 3
    AutreThe product fractions were collected
  4. 4
    Autrethe solvent was removed under vacuum

Mode opératoire

methyl 4-(4-chloro-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)-2-hydroxybenzoate (100 mg, 0.264 mmol), tert-butyl 6-hydroxyhexylcarbamate (68.9 mg, 0.317 mmol), Triphenylphosphine (139 mg, 0.528 mmol), were dissolved in DCM then DIAD (0.103 mL, 0.528 mmol) was added. The reaction was stirred for 16 h. The solvent was removed under vacuum and the crude product was purified by silica gel chromatography using 20% EtOAc/Hexanes. The product fractions were collected and the solvent was removed under vacuum to give 55 mg (36%) methyl 2-(6-(tert-butoxycarbonylamino)hexyloxy)-4-(4-chloro-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzoate.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08741884B2uspto-grants-2014_06