Lawesson's reagent → 6-bromo-8-chloro-3,4-dihydroquinoline-2(1H)-thione

HRID 1521624

Reaktionsgleichung

Reaktionsgleichung von HRID 1521624
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([Cl:12])[CH:11]=1)[NH:8][C:7](=O)[CH2:6][CH2:5]2.COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:23])=CC=1>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([Cl:12])[CH:11]=1)[NH:8][C:7](=[S:23])[CH2:6][CH2:5]2

Komponenten

4

Edukt 2

HCID 87949Lawesson's reagentHCID 709797726-Bromo-8-chloro-3,4-dihydroquinolin-2(1H)-one

Produkt 1

HCID 899616046-bromo-8-chloro-3,4-dihydroquinoline-2(1H)-thione

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

To a stirred solution of 6-bromo-8-chloro-3,4-dihydroquinolin-2(1H)-one (80-1; 10 g, 0.038 mol) in toluene (130 mL) was added Lawesson's reagent (7.7 g, 0.019 mol). Reaction mass was refluxed at 100° C. for 3 h. The reaction mixture was concentrated and directly purified by silica gel column chromatography to obtain title compound. 1H NMR (400 MHz, DMSO-d6) δ: 11.25 (s, 1H), 7.61-7.60 (d, J=2.4 Hz, 1H), 7.48 (s, 1H), 2.96-2.93 (m, 2H), 2.85-2.81 (m, 2H). MS (M+2): 277.

Aufarbeitung

  1. customReaction mass
  2. concentrationThe reaction mixture was concentrated
  3. customdirectly purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-82d59694bcf54d2a820b1e4ff8bb5270
Quelldatensatz
uspto-grants-2015_07
Patentnummer
US09073929B2

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