تفاعل #41750

ord-945600a21b344bfa9f19cec40e035232

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe mixture was then concentrated
  2. 2
    أخرىpartitioned between ethyl acetate and water
  3. 3
    تركيزThe organic layer was concentrated

الإجراء التجريبي

To 4-(2-{[4-chloro-3-(trifluoromethyl)phenylamino)-1-methylbenzimidazol-5-yloxy)pyridine-2-carboxylic acid (1 eq) in tetrahydrofuran was added 2-piperidylethylamine (2 eq), HBTU (2 eq) and N,N-diisopropylethylamine (4 eq) and stir at ambient temperature for 16 h. The mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was concentrated and preparative chromatography yielded [4-(2-{[4-chloro-3-trifluoromethylphenyl]amino-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-(2-piperidylethyl)carboxamide. MS: MH+=558.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07728010B2uspto-grants-2010_06