Réaction #649745

ord-3b4e1e39eb274b2eb2005a7bf9a17651

Équation de réaction

C1COCO1
dioxolane
Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)cc2)cc1Nc1nccc(-c2cccnc2)n1
Imatinib
C1COCO1
1,3-dioxolane
CS(=O)(=O)O
methanesulphonic acid
CS(=O)(=O)O.Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)cc2)cc1Nc1nccc(-c2cccnc2)n1
Imatinib Mesylate

Solvants

Conditions de réaction

Température
5°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONwas added
  2. 2
    workup.ADDITIONAfter addition the solution
  3. 3
    Températurewas cooled from 20° C.-10° C. in 1 hour and after 1 hour
  4. 4
    Températurewas cooled again from 10° C.-5° C. in 1 hour
  5. 5
    workup.STIRRINGThe suspension was stirred for 4 hours at 5° C
  6. 6
    workup.STIRRINGwithout stirring
  7. 7
    FiltrationThe suspension was filtered
  8. 8
    Lavagethe product was washed with 6 liters of 1,3-dioxolane

Mode opératoire

Imatinib base (600 g), 5.7 liters of 1,3-dioxolane and 300 ml of water were added to a vessel. The suspension was stirred at 20° C. for 15 minutes and than 113.3 g of methanesulphonic acid was added. After addition the solution was cooled from 20° C.-10° C. in 1 hour and after 1 hour of stirring the solution was cooled again from 10° C.-5° C. in 1 hour. The suspension was stirred for 4 hours at 5° C. Than 6 liters of dioxolane was added in 30 minutes maintaining the temperature at 5° C. The suspension was left for 2.5 hours at 5° C. without stirring. The suspension was filtered and the product was washed with 6 liters of 1,3-dioxolane.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08067421B2uspto-grants-2011_11