Reacción #63731

ord-d7bdef4d67254c71b6bd0a37201da9a6

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónAfter concentrating the mixture the residue
  2. 2
    workup.DISSOLUTIONdissolved in methylene chloride, whereupon 10% sodium bicarbonate solution
  3. 3
    workup.ADDITIONis added
  4. 4
    Extracciónthe mixture is extracted
  5. 5
    Secadothe methylene chloride solutlon is dried
  6. 6
    Concentraciónconcentrated
  7. 7
    OtroThe thus-obtained crude product
  8. 8
    Otrois chromatographed on silica gel
  9. 9
    Otropurified with methylene chloride/ethyl acetate (1:1)
  10. 10
    Otrothe pressure being produced with nitroqen gas

Procedimiento

A suspension of 5.2 g of 5.7-dihydro-2-mercapto-5,5,7,7 -tetramethylindeno[5,6-d]imidazol-6(1H )-one and 2.6 g of potassium t-butanolate is treated under argon with a solution of 3 g of 2-chloromethyl-3-methylpyridine in 30 ml of t-butanol and the mixture is stirred for 18 hours. After concentrating the mixture the residue is acidified with glacial acetic acid and dissolved in methylene chloride, whereupon 10% sodium bicarbonate solution is added thereto. the mixture is extracted and the methylene chloride solutlon is dried and concentrated. The thus-obtained crude product is chromatographed on silica gel and purified with methylene chloride/ethyl acetate (1:1), the medium pressure flash chromatography method being used and the pressure being produced with nitroqen gas. The 5,7-dihydro-5,5,7,7-tetramethyl-2-[[(3-methyl-2 -pyridyl)methyl]thio]indeno[5,6-d]imidazol-6(1H )-one which is obtained from ethyl acetate-n-hexane melts at 161°-164°.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04766133uspto-grants-1988_08