Reaktion #1844470

ord-8203257a05404fa9b0e833f839e0b4b4

Reaktionsgleichung

CCC1=Nc2ccccc2C(=O)C1
2-ethyl-4-quinolone
c1ccc(C(c2ccccc2)(c2ccccc2)c2nnn[nH]2)cc1
III
c1ccc(C(c2ccccc2)(c2ccccc2)c2nnn[nH]2)cc1
triphenylmethyl tetrazole
Nc1ccccc1
aniline
CCC(=O)CC(=O)OC
methyl propionylacetate
CCCc1cc(OCc2ccc(-c3ccccc3-c3nnn(C(c4ccccc4)(c4ccccc4)c4ccccc4)n3)cc2)c2ccccc2n1
4'-bromomethylbiphenyl-2-carbonitrile
CCCc1cc(OCc2ccc(-c3ccccc3-c3nnn(C(c4ccccc4)(c4ccccc4)c4ccccc4)n3)cc2)c2ccccc2n1
2-propyl-4-[(2'-(2-triphenylmethyl-2H-tetrazol-5-yl)biphenyl-4-yl)methoxy]quinoline
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCc1cc(OCc2ccc(-c3ccccc3C#N)cc2)c2ccccc2n1
4'-[(2-ethylquinolin-4-yloxy)methyl]-biphenyl-2-carbonitrile
Ausbeute 111.6%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstige(prepared by a similar method to
  2. 2
    FiltrationThe suspended solid was collected by filtration
  3. 3
    Waschenwashed with water
  4. 4
    Sonstigedried at 60° C. under vacuum
  5. 5
    SonstigeThe solid was recrystallised from tert-butyl methyl ether

Vorschrift

A mixture of 2-ethyl-4-quinolone (1.73 g), (prepared by a similar method to that described in Org. Syn., Coll. Vol. III, p.374 and p.593 from aniline and methyl propionylacetate), 4'-bromomethylbiphenyl-2-carbonitrile (A) (3.1 g) and solid potassium carbonate (1.81 g) in N-methylpyrrolidone (40 ml) were stirred for 36 hours under nitrogen. The mixture was then added dropwise to water (100 ml) at 15°-25° C. and stirred for 30 minutes. The suspended solid was collected by filtration, washed with water, and dried at 60° C. under vacuum. The solid was recrystallised from tert-butyl methyl ether to give 4'-[(2-ethylquinolin-4-yloxy)methyl]-biphenyl-2-carbonitrile as a solid (1.9 g), m.p. 151°-153° C.; NMR(CDCl3): 1.4(t, 3H), 2.97(q,2H), 5.35(s,2H), 6.76(s,1H), 7.4-7.6(m, 3H), 7.6-7.8(m, 6H), 8.0(d, 1H), 8.25(d, 1H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05444071uspto-grants-1995_08