반응 #428436

ord-b4107e4f375241158650d5c5099d22d5

반응 방정식

O=C(O)c1ccc(-c2ccncc2)cc1
4-(pyridin-4-yl)benzoic acid
COc1cccc([C@H](C)N)c1
(S)-1-(3-methoxyphenyl)ethanamine
CCN(C(C)C)C(C)C
DIEA
CN(C)C(On1nnc2ccccc21)=[N+](C)C.F[B-](F)(F)F
O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate
COc1cccc([C@H](C)NC(=O)c2ccc(-c3ccncc3)cc2)c1
title compound
수율 66.3%
COc1cccc([C@H](C)NC(=O)c2ccc(-c3ccncc3)cc2)c1
N—[(S)-1-(3-methoxy-phenyl)-ethyl]-4-pyridin-4-yl-benzamide
수율 66.3%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed with 1N NaOH
  2. 2
    건조dried (Na2SO4)
  3. 3
    기타chromatographed (20-85% EtOAc/dichloromethane)
  4. 4
    기타triturated (Et2O)

실험 절차

A mixture of 4-(pyridin-4-yl)benzoic acid (0.970 g, 4.87 mmol), (S)-1-(3-methoxyphenyl)ethanamine (0.884 g, 5.84 mmol), DIEA (1.7 ml, 9.8 mmol), and O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (1.87 g, 5.82 mmol) in DMF (10 ml) was stirred overnight, diluted with EtOAc, washed with 1N NaOH, sat NaHCO3, and brine, dried (Na2SO4), and chromatographed (20-85% EtOAc/dichloromethane) and triturated (Et2O) to give the title compound (1.075 g, 3.23 mmol) as a white solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08895749B2uspto-grants-2014_11