Reacción #2122477

ord-12a6ba47f0fb4e34b5aa8bf0f6bf5365

Ecuación de reacción

O=C(O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@@H]21
Biotin
C1CNCCN1
piperazine
c1ccncc1
pyridine
NC(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@@]21N1CCNCC1
piperazine biotinamide
Rendimiento 10.0%

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas removed
  2. 2
    Otrodried down
  3. 3
    workup.ADDITIONwas added to the resulting oil
  4. 4
    Concentraciónconcentrated
  5. 5
    Otrothe resulting solid was triturated with 40 mL of MeOH
  6. 6
    FiltraciónThe MeOH soluble material was collected by filtration
  7. 7
    Concentraciónconcentrated
  8. 8
    Otrotriturated with 40 ml of CH2Cl2
  9. 9
    FiltraciónThe CH2Cl2 soluble material was collected by filtration
  10. 10
    Concentraciónconcentrated
  11. 11
    Otrochromatographed on a 1 cm silica column with 2:98 NH4OH
  12. 12
    LavadoElution
  13. 13
    ConcentraciónThe appropriate fractions were concentrated

Procedimiento

Biotin (0.34 g, 1.4 mmols) was dissolved in 8 mL of neat thionyl chloride. This reaction was allowed to proceed for 5 min before the reaction was placed under vacuum where excess thionyl chloride was removed. The resulting oil was resuspended in 10 mL of CH2Cl2 and dried down. This process was repeated three times in order to drive off excess thionyl chloride. A solution of piperazine (0.54 g, 6.3 mmols) dissolved in 30 mL of pyridine was added to the resulting oil. This solution was stirred overnight, concentrated and the resulting solid was triturated with 40 mL of MeOH. The MeOH soluble material was collected by filtration, concentrated, and triturated with 40 ml of CH2Cl2. The CH2Cl2 soluble material was collected by filtration, concentrated and chromatographed on a 1 cm silica column with 2:98 NH4OH:ethanol as the running solvent. Elution was monitored by TLC where the product displays an Rf of 0.80 with a 33:67 NH4OH:EtOH developing solution. The appropriate fractions were concentrated to give 42.9 mg of the piperazine biotinamide as a white solid in a 10% yield.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08574546B2uspto-grants-2013_11