تفاعل #2446152

ord-c9b13ac12bb6469f8cd85d5af8479b54

معادلة التفاعل

O=C1CCc2cc(-c3cccnc3)ccc2N1
6-Pyridin-3-yl-3,4-dihydro-1H-quinolin-2-one
COc1ccc(P2(=S)SP(=S)(c3ccc(OC)cc3)S2)cc1
Lawessons reagent
S=C1CCc2cc(-c3cccnc3)ccc2N1
6-Pyridin-3-yl-3,4-dihydro-1H-quinoline-2-thione

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter evaporation of the solvent under reduced pressure
  2. 2
    أخرىthe residue was purified by flash chromatography on silica gel (hexanes/ethyl acetate, 3/7, Rf=0.31) which

الإجراء التجريبي

A mixture of 6-Pyridin-3-yl-3,4-dihydro-1H-quinolin-2-one (395 mg, 1.76 mmol) and Lawessons reagent (356 mg, 0.88 mmol) was refluxed in 30 ml toluene for 2 h. After evaporation of the solvent under reduced pressure, the residue was purified by flash chromatography on silica gel (hexanes/ethyl acetate, 3/7, Rf=0.31) which gave 6-Pyridin-3-yl-3,4-dihydro-1H-quinoline-2-thione as yellow plates (63 mg, 0.26 mmol, 15%), mp (hexanes/ethyl acetate) 267° C. 1H-NMR (500 MHz, DMSO-d6): δ=2.87 (m, 2H), 2.97 (m, 2H), 7.20 (d, 3J=8.2 Hz, 1H), 7.46 (dd, 3J=7.9 Hz, 3J=4.6 Hz, 1H), 7.59 (dd, 3J=8.2 Hz, 4J=1.9 Hz, 1H), 7.62 (d, 4J=1.9 Hz, 1H), 8.04 (m, 1H), 8.53 (dd, 3J=4.7 Hz, 4J=1.6 Hz, 1H), 8.87 (d, 4J=2.2 Hz, 1H), 12.30 (s, 1H). MS m/z=241.05 (MH+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08685960B2uspto-grants-2014_04