تفاعل #8698

ord-50ab374672784712afdda58eb7ef9ef4

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىBulk of the solvent was evaporated before it
  2. 2
    workup.ADDITIONwas diluted with diethyl ether (50 ml)
  3. 3
    أخرىThe precipitate that formed
  4. 4
    أخرىwas collected
  5. 5
    غسيلwashed with diethyl ether (100 ml)
  6. 6
    أخرىdried

الإجراء التجريبي

A solution of 4,6-dichloro-5-(2-methoxyphenoxy)-2-(4-pyridyl)-pyrimidine (2 g) and 2-phenyl-ethanesulfonic acid amide potassium salt (2.82 g, Referential Example 1e) in DMF (50 ml) was stirred at rt for 16 h. Bulk of the solvent was evaporated before it was diluted with diethyl ether (50 ml). The mixture was acidified with 10% aq. citric acid. The precipitate that formed was collected, washed with diethyl ether (100 ml) and dried to give 2-phenyl-ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amide (2.23 g) as a beige powder. LC-MS: tR=4.93 min, [M+1]+=497.22, [M−1]−=494.96.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091201B2uspto-grants-2006_08