تفاعل #10343

ord-101c7ac50baf4d4999c44b012e398b23

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىprepared from the product
  2. 2
    أخرىfollowed by the evaporation of the solvent]
  3. 3
    workup.ADDITIONthen poured onto water (300 ml) and diethylether (120 ml)
  4. 4
    workup.ADDITIONwas added
  5. 5
    workup.STIRRINGthe solution was stirred for 30 min
  6. 6
    أخرىThe layers were separated
  7. 7
    درجة الحرارةcooled to 0° C. for 1 h
  8. 8
    ترشيحThe precipitated product was filtered off
  9. 9
    غسيلwashed with water
  10. 10
    أخرىrecrystallized from methanol

الإجراء التجريبي

To 4,6-dichloro-5-(4-chloro-phenyl)-pyrimidine (Referential Example 9) (2.59 g) dissolved in DMSO (14 ml) was added di-isopropyl-ethyl-amine (1.8 ml) followed by the addition of benzyl sulfamic acid amide potassium salt (2.25 g) [prepared from the product described in Referential Example 22 and potassium tert.-butylate in methanol followed by the evaporation of the solvent]. The mixture was stirred for 24 h at rt then poured onto water (300 ml) and diethylether (120 ml) was added and the solution was stirred for 30 min. The layers were separated and the water layer was acidified with solid citric acid (pH=3) and cooled to 0° C. for 1 h. The precipitated product was filtered off, washed with water and recrystallized from methanol to give benzyl sulfamic acid-[6-chloro-5-(p-chloro-phenyl)-4-pyrimidinyl]-amide (1.8 g). tR=4.94 min (LC); [M+H]+410.90 (ES+);

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07094781B2uspto-grants-2006_08