Lawesson's reagent → 8-Chloro-6-pyridin-3-yl-3,4-dihydroquinoline-2(1H)-thione

HRID 44193

Reaktionsgleichung

Reaktionsgleichung von HRID 44193
[Cl:1][C:2]1[CH:3]=[C:4]([C:13]2[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=2)[CH:5]=[C:6]2[C:11]=1[NH:10][C:9](=O)[CH2:8][CH2:7]2.COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:28])=CC=1.CC(C)=O.C(OCC)C>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:3]=[C:4]([C:13]2[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=2)[CH:5]=[C:6]2[C:11]=1[NH:10][C:9](=[S:28])[CH2:8][CH2:7]2

Komponenten

5

Edukt 3

HCID 87949Lawesson's reagentHCID 21584533Acetone diethyletherHCID 251802998-Chloro-6-pyridin-3-yl-3,4-dihydroquinolin-2(1H)-one

Produkt 1

HCID 251805048-Chloro-6-pyridin-3-yl-3,4-dihydroquinoline-2(1H)-thione

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

A mixture of 8-chloro-6-pyridin-3-yl-3,4-dihydro-1H-quinolin-2-one (900 mg, 3.48 mmol) and Lawessons reagent (985 mg, 2.44 mmol) was refluxed in 50 ml toluene for 2 h. After evaporation of the solvent under reduced pressure, the residue was purified by flash chromatography on silica gel (ethyl acetate, Rf=0.26) and crystallization from acetone/diethylether. 8-Chloro-6-pyridin-3-yl-3,4-dihydro-1H-quinoline-2-thione was obtained as yellow needles (212 mg, 0.77 mmol, 22%), mp (acetone/diethylether) 175° C. 1H-NMR (500 MHz, DMSO-d6): δ=2.91 (m, 2H), 3.00 (m, 2H), 7.46 (ddd, 3J=7.9 Hz, 3J=4.9 Hz, 5J=0.9 Hz, 1H), 7.66 (d, 4J=2.1 Hz, 1H), 7.76 (d, 4J=2.0 Hz, 1H), 8.09 (ddd, 3J=7.9 Hz, 4J=2.4 Hz, 4J=1.5 Hz, 1H), 8.56 (dd, 3J=4.9 Hz, 4J=1.5 Hz, 1H), 8.91 (dd, 4J=2.4 Hz, 5J=0.9 Hz, 1H), 11.31 (bs, 1H). 13C-NMR (125 MHz, DMSO-d5): δ=25.6, 39.4, 120.5, 123.8, 125.2, 126.0, 129.7, 133.4, 133.6, 133.8, 133.9, 147.5, 148.8, 201.5. MS m/z=273.95 (M35Cl+), 275.95 (M37Cl+).

Aufarbeitung

  1. customAfter evaporation of the solvent under reduced pressure
  2. customthe residue was purified by flash chromatography on silica gel (ethyl acetate, Rf=0.26) and crystallization from acetone/diethylether

Quellen und Nachweise

ORD-Eintrag
ord-2392b5ed779c46aa95a540b73d55787f
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08541404B2

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