Reacción #73252

ord-290f931e8cc043eeb5a60b9b45b795c8

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe reaction to a dark solution
  2. 2
    ConcentraciónThe reaction was then concentrated
  3. 3
    Otroto remove the DCM
  4. 4
    workup.ADDITIONthe resulting DMF solution was diluted with water
  5. 5
    Otroto precipitate the product
  6. 6
    OtroThe solid precipitate was collected
  7. 7
    Lavadowashed with water
  8. 8
    Otroto give a dark solid
  9. 9
    Lavadowashed with brine
  10. 10
    Secadodried over magnesium sulfate
  11. 11
    Concentraciónconcentrated
  12. 12
    Otroto give a very dark oily residue
  13. 13
    workup.STIRRINGThis was stirred at rt
  14. 14
    Otroto precipitate 3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]-pyrimidin-4-yl)-1H-pyrazol-1-yl]pentanedinitrile as white needle-like crystals (22.7 gm, 85%), LC/MS (M+H)+

Procedimiento

3-[4-(7-[2-(Trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]pentanediamide (29.0 g, 0.0654 mol) was partially dissolved in DMF (200 mL, 2 mol), DCM (200 mL, 3 mol) and TEA (36 mL, 0.26 mol) and cooled in an ice bath under nitrogen atmosphere. The trichloroacetyl chloride (15 mL, 0.14 mol) was added dropwise turning the reaction to a dark solution. This was stirred at 0° C. for ½ h. The reaction was then concentrated to remove the DCM and the resulting DMF solution was diluted with water to precipitate the product. The solid precipitate was collected and washed with water to give a dark solid. The solid was then dissolved in DCM and washed with brine, dried over magnesium sulfate and concentrated to give a very dark oily residue. The residue was taken up in DCM, and hexane was added until the solution became slightly cloudy. This was stirred at rt to precipitate 3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]-pyrimidin-4-yl)-1H-pyrazol-1-yl]pentanedinitrile as white needle-like crystals (22.7 gm, 85%), LC/MS (M+H)+: 408, 1H NMR (DMSO-d6) δ 9.07 (s, 1H), 8.87 (s, 1H), 8.59 (s, 1H), 7.88 (d, 1H), 7.19 (d, 1H), 5.75 (s, 2H), 5.30 (m, 1H), 3.62 (t, 2H), 3.40 (m, 4H), 0.91 (t, 2H), 0.10 (s, 9H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08541425B2uspto-grants-2013_09