Reacción #73206

ord-09d70c7c6c744c7e88c80d45b4ad32b5

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe mixture was then concentrated in vacuo
  2. 2
    ConcentraciónThe mixture was then concentrated
  3. 3
    workup.ADDITIONthe residue was diluted with water
  4. 4
    Extracciónextracted with several portions of 15% IPA/CH2Cl2
  5. 5
    SecadoThe combined extracts were dried over sodium sulfate
  6. 6
    Concentraciónconcentrated in vacuo

Procedimiento

A solution of 3-methyl-3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butan-1-ol (13.8 g, 0.0344 mol) in TFA (20 mL) was stirred for 1 hour. The mixture was then concentrated in vacuo and the residue was stirred for 2 hours in a mixture of methanol (30 mL), ammonium hydroxide (30 mL), and ethylenediamine (8 mL). The mixture was then concentrated, and the residue was diluted with water and extracted with several portions of 15% IPA/CH2Cl2. The combined extracts were dried over sodium sulfate and concentrated in vacuo to give 20 g of white solid. The solid was triturated with ether and the product was isolated by filtration to give the product as a white solid (7.75 g, 83%).

Fuente

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