3-Nitrophenylboronic Acid → 6-(4-methoxyphenyl)-3-(3-nitrophenyl)-9H-pyrido[2,3-b]indole

HRID 341299Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 341299
Cl[C:2]1[CH:22]=[N:21][C:5]2[NH:6][C:7]3[C:12]([C:4]=2[CH:3]=1)=[CH:11][C:10]([C:13]1[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=1)=[CH:9][CH:8]=3.[N+:23]([C:26]1[CH:27]=[C:28](B(O)O)[CH:29]=[CH:30][CH:31]=1)([O-:25])=[O:24].[O-]P([O-])([O-])=O.[K+].[K+].[K+].COC1C=CC=C(OC)C=1C1C=CC=CC=1P(C1CCCCC1)C1CCCCC1>CC([O-])=O.CC([O-])=O.[Pd+2]>[CH3:20][O:19][C:16]1[CH:17]=[CH:18][C:13]([C:10]2[CH:11]=[C:12]3[C:7](=[CH:8][CH:9]=2)[NH:6][C:5]2[N:21]=[CH:22][C:2]([C:30]4[CH:29]=[CH:28][CH:27]=[C:26]([N+:23]([O-:25])=[O:24])[CH:31]=4)=[CH:3][C:4]3=2)=[CH:14][CH:15]=1

Komponenten

6

Versuchsvorschrift

3-chloro-6-(4-methoxyphenyl)-9H-pyrido[2,3-b]indole (50 mg, 0.16 mmol, 1 equiv.), 3-nitrophenylboronic acid (81 mg, 0.48 mmol, 3 equiv.), K3PO4 (136 mg, 0.64 mmol, 4 equiv.), S-PHOS (13.1 mg, 0.032 mmol, 0.2 equiv.), Pd(OAc)2 (4.0 mg, 0.016 mmol, 0.1 equiv.) are introduced in a schlenk tube which is flushed with N2. Freshly distilled dioxane (0.433 ml) is then injected and the reaction is carried out at 100° C. overnight. The mixture is filtered through celite and concentrated under reduced pressure. The crude product is purified over silica gel chromatography (eluant CH2Cl2/AcOEt 6:4). The white solid obtained is washed with methanol to give the product as a white solid (43 mg, 0.11 mmol) in 69% yield.

Aufarbeitung

  1. customis flushed with N2
  2. filtrationThe mixture is filtered through celite and
  3. concentrationconcentrated under reduced pressure
  4. customThe crude product is purified over silica gel chromatography (eluant CH2Cl2/AcOEt 6:4)
  5. customThe white solid obtained
  6. washis washed with methanol

Quellen und Nachweise

ORD-Eintrag
ord-c33189b364bf4cdaac7ef339b773dc62
Quelldatensatz
uspto-grants-2014_11
Patentnummer
US08895744B2

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