반응 #5776

ord-19b3524e42254cd798a618b4d5e376b5

반응 방정식

CCN(CC)CC
Triethylamine
CCc1cc(OCc2ccc(B(O)O)cc2)c2ccccc2n1.Cl
4-[(2-ethylquinolin-4-yloxy)methyl]phenylboronic acid hydrochloride
N#Cc1ccccc1Br
2-bromobenzonitrile
CCc1cc(OCc2ccc(-c3ccccc3C#N)cc2)c2ccccc2n1
4'-[(2-ethylquinolin-4-yloxy)methyl]biphenyl-2-carbonitrile
수율 91.1%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the mixture was heated
  2. 2
    온도at reflux for 3 hours
  3. 3
    여과The hot reaction mixture was filtered through diatomaceous earth
  4. 4
    온도The mixture was then cooled to 4° C. for 30 minutes
  5. 5
    기타The solid which crystallised
  6. 6
    여과was collected by filtration
  7. 7
    세척washed with cold butanol (16 ml) and water (2×16 ml)
  8. 8
    기타dried at 55° C.

실험 절차

Triethylamine (13.8 ml) was added to a mixture of 4-[(2-ethylquinolin-4-yloxy)methyl]phenylboronic acid hydrochloride (12.74 g), 2-bromobenzonitrile (5.92 g) and palladium chloride (0.13 g) in butanol (80 ml) and water (40 ml) and the mixture was heated at reflux for 3 hours. The hot reaction mixture was filtered through diatomaceous earth and the filtrate was stirred while allowing to cool to ambient temperature. The mixture was then cooled to 4° C. for 30 minutes. The solid which crystallised was collected by filtration, washed with cold butanol (16 ml) and water (2×16 ml) and then dried at 55° C. to give 4'-[(2-ethylquinolin-4-yloxy)methyl]biphenyl-2-carbonitrile (10.8 g); m.p. 161°-162° 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,1 H), 8.25(d,1H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05245035uspto-grants-1993_09