Reacción #1687622

ord-60edf243ccb0493086a32b0c8e78a6a2

Ecuación de reacción

Cn1nnc(-c2cccnc2)n1
12
Cn1nnc(-c2cccnc2)n1
2-Methyl-5-(3-pyridyl)-2H-tetrazole
Cl
hydrogen chloride
Cl.Cn1nnc(C2CCCNC2)n1
title product
Rendimiento 26.0%
Cl.Cn1nnc(C2CCCNC2)n1
2-Methyl-(3-piperidyl)-2H-tetrazole, hydrochloride
Rendimiento 26.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrountil acidic reaction
  2. 2
    FiltraciónThe precipitate was filtered off
  3. 3
    Otrodried
  4. 4
    workup.DISSOLUTIONdissolved in methanol (25 ml)
  5. 5
    workup.ADDITION5% palladium on charcoal (0.6 g) was added
  6. 6
    FiltraciónThe catalyst was filtered off
  7. 7
    Otrothe filtrate was evaporated to dryness
  8. 8
    OtroCrystallization from ethanol

Procedimiento

To a solution of 12 (1.93 g, 0.012 mol) in acetone (50 ml) was added hydrogen chloride in ether until acidic reaction. The precipitate was filtered off, dried, and dissolved in methanol (25 ml). 5% palladium on charcoal (0.6 g) was added, and the mixture was shaked overnight under 3 atm. of hydrogen pressure. The catalyst was filtered off and the filtrate was evaporated to dryness. Crystallization from ethanol yielded 0.63 g (0.0031 mol, 26%) of title product M.P. 168°-172° C. Anal. (C7H14ClN5) C, H, N.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE036374uspto-grants-1999_11