Reacción #2507849

ord-e4b91c21c5274719a6e03c691ce48664

Ecuación de reacción

NS(=O)(=O)O
Sulfamic acid
Nc1cccc(-c2cccc(C(=O)O)c2)c1O
3′-Amino-2′-hydroxybiphenyl-3-carboxylic acid
Cc1cc(O)n(-c2ccc(C)c(C)c2)n1
1-(3,4-dimethylphenyl)-3-methyl-1H-pyrazol-5-ol
Cl
Hydrochloric acid
Cl
hydrochloric acid
O=N[O-].[Na+]
sodium nitrite
CC1=NN(c2ccc(C)c(C)c2)C(=O)/C1=N\Nc1cccc(-c2cccc(C(=O)O)c2)c1O
Eltrombopag
Rendimiento 95.4%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGThe resulting red solution was stirred for thirty minutes
  2. 2
    TemperaturaThe solution was then cooled to 0-5° C.
  3. 3
    Otrodid not rise above 10° C
  4. 4
    workup.STIRRINGThe reaction mixture was stirred for one hour at 5-10° C
  5. 5
    workup.STIRRINGthe resulting mixture was stirred for additionally one hour at the same temperature
  6. 6
    TemperaturaThe reaction mixture was warmed to room temperature
  7. 7
    workup.STIRRINGthe resulting mixture was stirred for additionally two hours at room temperature
  8. 8
    workup.STIRRINGwith stirring over twenty minutes
  9. 9
    OtroA solid precipitated
  10. 10
    Filtraciónwas collected by filtration
  11. 11
    Lavadowashed with of mixture MeOH:water (1:1, 100 mL)
  12. 12
    Otrodried at 40° C./0 bar in vacuum oven for about 18 hours

Procedimiento

3′-Amino-2′-hydroxybiphenyl-3-carboxylic acid (“BPCA”) Form I (90 g, 392.6 mmol), was added slowly with stirring at room temperature to a solvent mixture of tech. methanol (1.8 L) and 4 M hydrochloric acid (0.245 L, 981.5 mmol) in 3 L reactor. The resulting red solution was stirred for thirty minutes. The solution was then cooled to 0-5° C. and a cold solution of sodium nitrite (27 g, 391.3 mmol) in 90 mL of water was added over twenty minutes such that the reaction mixture temperature did not rise above 10° C. The reaction mixture was stirred for one hour at 5-10° C. Sulfamic acid (4 g, 41.2 mmol) in 90 mL of water was added at 5° C. and the resulting mixture was stirred for additionally one hour at the same temperature. The reaction mixture was warmed to room temperature and triethylamine (ca 104 mL) was added to adjust pH 7-8. 1-(3,4-dimethylphenyl)-3-methyl-1H-pyrazol-5-ol (“pyrazole”) form I (72 g, 357.8 mmol), was added in one portion to the reaction mixture and the resulting mixture was stirred for additionally two hours at room temperature. Hydrochloric acid (4M, ca 140 mL) was slowly added with stirring over twenty minutes to adjust pH to 1.8. A solid precipitated and was collected by filtration, washed with of mixture MeOH:water (1:1, 100 mL) and dried at 40° C./0 bar in vacuum oven for about 18 hours giving 151 g of crude orange to brown crystals of Eltrombopag crude (XRPD: form III with small percentage (less than 10%) of form I. (HPLC: 98.5%, Yield=95.4%)

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07956048B2uspto-grants-2011_06