Reacción #49813

ord-cb7cb858867743fd95b620cbded84999

Ecuación de reacción

CC(C)OC(=O)N1c2cncnc2NC(=O)C1C
(2RS)-1-(isopropoxycarbonyl)-2-methyl-1,2-dihydro-1,4,5,7-tetraazanaphthalen-3(4H)-one
CC(C)OC(=O)N1c2cncnc2NC(=O)C1C
(2RS)-1-(Isopropoxycarbonyl)-2-methyl-1,2-dihydro-1,4,5,7-tetraazanaphthalen-3(4H)-one
COc1ccc(P2(=S)SP(=S)(c3ccc(OC)cc3)S2)cc1
Lawesson's reagent
CC(C)OC(=O)N1c2cncnc2NC(=S)C1C
desired compound
Rendimiento 28.0%
CC(C)OC(=O)N1c2cncnc2NC(=S)C1C
(2RS)-1-(Isopropoxycarbonyl)-2-methyl-1,2-dihydro-1,4,5,7-tetraazanaphthalene-3(4H)-thione
Rendimiento 28.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe crude product after concentration
  2. 2
    Otrowas chromatographed (silica gel; ethyl acetate/heptane=1:1)

Procedimiento

100 mg of (2RS)-1-(isopropoxycarbonyl)-2-methyl-1,2-dihydro-1,4,5,7-tetraazanaphthalen-3(4H)-one from Example 24 were reacted with Lawesson's reagent in analogy to Example 20. The crude product after concentration was chromatographed (silica gel; ethyl acetate/heptane=1:1). 30 mg (28%) of the desired compound, of melting point 203°-204° C., were obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05424311uspto-grants-1995_06