Реакция #218879

ord-fca679a05960494fb0deada487f00d6f

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

N-Ethyl-2′-methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(4-phenoxybenzyl)-1,1′-biphenyl-4-carboxamide was prepared from 2′-methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(4-phenoxybenzyl)-1,1′-biphenyl-4-carboxamide and iodoethane using method L. NMR; δH [2H6]—DMSO 7.89,(1H, d), 776,(1H, s), 7.55-7.48,(5H, m), 7.40-7.36,(3H, m), 7.24,(1H, b), 7.13,(1H, t), 7.00,(4H, m), 4.694.51,(2H, m), 3.39-3.22,(2H, m), 2.55,(3H, s), 2.31,(3H, s), 1.08,(3H, b). LCMS; retention time 3.93 min, MH+ 504.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07384963B2uspto-grants-2008_06