تفاعل #1810825

ord-a34d60c3c9974d9c9c4c246be92744d3

معادلة التفاعل

CS(=O)(=O)c1ccc(OCC(F)(F)F)c(C(=O)O)c1
5-methanesulfonyl-2-(2,2,2-trifluoro-ethoxy)-benzoic acid
CN(C)C(On1nnc2ccccc21)=[N+](C)C.F[B-](F)(F)F
TBTU
CCN(C(C)C)C(C)C
N-ethyldiisopropylamine
FC(F)(F)c1ccc(C2=CCNCC2)cc1
4-(4-trifluoromethyl-phenyl)-1,2,3,6-tetrahydro-pyridine
CS(=O)(=O)c1ccc(OCC(F)(F)F)c(C(=O)N2CC=C(c3ccc(C(F)(F)F)cc3)CC2)c1
title compound
CS(=O)(=O)c1ccc(OCC(F)(F)F)c(C(=O)N2CC=C(c3ccc(C(F)(F)F)cc3)CC2)c1
[5-Methanesulfonyl-2-(2,2,2-trifluoro-ethoxy)-phenyl]-[4-(4-trifluoromethyl-phenyl)3,6-dihydro-2H-pyridin-1-yl]-methanone

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزconcentrated in vacuo
  2. 2
    أخرىpurified by column chromatography (SiO2, 10 g, heptane, ethylacetate 0 to 100%)

الإجراء التجريبي

To a solution of 0.17 mmol 5-methanesulfonyl-2-(2,2,2-trifluoro-ethoxy)-benzoic acid in 0.75 ml dimethylformamide, 0.19 mmol TBTU, 0.855 mmol N-ethyldiisopropylamine and 0.205 mmol 4-(4-trifluoromethyl-phenyl)-1,2,3,6-tetrahydro-pyridine were successively added. The reaction was then stirred at RT for 45 min., concentrated in vacuo and purified by column chromatography (SiO2, 10 g, heptane, ethylacetate 0 to 100%), to give the title compound. MS (m/e): 508.6 (MH+, 100%)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07485637B2uspto-grants-2009_02