Реакция #10342

ord-74338b5aed30449facdcc0ace8215f09

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеprepared from the product
  2. 2
    Другоеfollowed by evaporation of the solvent]
  3. 3
    workup.ADDITIONthen poured onto water (500 ml) and diethylether (250 ml)
  4. 4
    workup.ADDITIONwas added
  5. 5
    workup.STIRRINGthe solution was stirred for 30 min
  6. 6
    ДругоеThe layers were separated
  7. 7
    Температураcooled to 0° C. for 1 h
  8. 8
    ФильтрацияThe precipitated product was filtered off
  9. 9
    Промывкаwashed with water and diethylether
  10. 10
    Другоеdried

Методика

To 4,6-dichloro-5-p-tolyl-pyrimidine (Referential Example 7) (2.0 g) dissolved in DMSO (35 ml) was added di-isopropyl-ethyl-amine (1.46 ml) followed by addition of 4-methyl-phenyl sulfamic acid amide potassium salt (2.78 g) [prepared from the product described in Referential Example 19 and potassium tert.-butylate in methanol followed by evaporation of the solvent]. The mixture was stirred for 48 h at rt then poured onto water (500 ml) and diethylether (250 ml) was added and the solution was stirred for 30 min. The layers were separated and the water layer was acidified with acetic acid (2.0 ml) and cooled to 0° C. for 1 h. The precipitated product was filtered off and washed with water and diethylether and dried to give 4-methyl-phenyl sulfamic acid-[6-chloro-5-(p-tolyl)-4-pyrimidinyl]-amide (2.02 g). tR=5.00 min (LC); [M+H]+=389.11 (ES+);

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07094781B2uspto-grants-2006_08