反应 #2507851

ord-9c9becc32b6c4cd0824c4c99ff13ee75

反应方程式

CC1=NN(c2ccc(C)c(C)c2)C(=O)/C1=N\Nc1cccc(-c2cccc(C(=O)O)c2)c1O
Eltrombopag
NCCO
Ethanolamine
NCCO
ethanolamine
O
Water
CC1=NN(c2ccc(C)c(C)c2)C(=O)/C1=N\Nc1cccc(-c2cccc(C(=O)O)c2)c1O.NCCO
title compound
收率 96.0%
CC1=NN(c2ccc(C)c(C)c2)C(=O)/C1=N\Nc1cccc(-c2cccc(C(=O)O)c2)c1O.NCCO
Eltrombopag ethanolamine
收率 96.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度to maintain a temperature greater
  2. 2
    其他28° C
  3. 3
    workup.ADDITIONWhen addition
  4. 4
    其他was returned to 30° C.
  5. 5
    过滤the solution filtered through a glass fiber pad (2× Whatman GFC filters)
  6. 6
    其他to remove particulate matter
  7. 7
    洗涤The filter was washed through with THF (2.0 ml) which
  8. 8
    workup.ADDITIONwas added to the filtrate
  9. 9
    workup.ADDITIONThe filtrate containing the free acid
  10. 10
    workup.STIRRINGThe resulting dark red suspension was stirred for 3 hours
  11. 11
    其他the solid isolated by filtration
  12. 12
    其他dried at 50° C. in a vacuum oven over night

实验过程

Eltrombopag crude orange solid (1 g) was stirred in 16.75 ml of THF at approximately 30° C. Water (2.0 ml) was added slowly so as to maintain a temperature greater then 28° C. When addition was complete, the temperature was returned to 30° C. and the solution filtered through a glass fiber pad (2× Whatman GFC filters) to remove particulate matter. The filter was washed through with THF (2.0 ml) which was added to the filtrate. The filtrate was allowed to cool to room temperature. Ethanolamine (0.324 g, 2.35 mol. equiv.) was dissolved in IMS (26 ml) at 22° C. and stirred under a nitrogen atmosphere at 22° C. The filtrate containing the free acid was added to the ethanolamine solution over 20 to 30 minutes. The resulting dark red suspension was stirred for 3 hours and the solid isolated by filtration and dried at 50° C. in a vacuum oven over night to yield 1.22 g (96%) of the title compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07956048B2uspto-grants-2011_06