Reacción #2122517

ord-4fed63a882874f0f944deba2d3468fac

Ecuación de reacción

Cc1nc2ccc(S(=O)(=O)Cl)cc2s1
Compound 2
Cc1nc2ccc(S(=O)(=O)Cl)cc2s1
2-methylbenzothiazole-6-sulfonyl chloride
CCCCCCNCCCCCC
dihexylamine
CCCCCC
hexane
CCCCCCN(CCCCCC)S(=O)(=O)c1ccc2nc(C)sc2c1
Compound 20
Rendimiento 97.0%
CCCCCCN(CCCCCC)S(=O)(=O)c1ccc2nc(C)sc2c1
N,N-dihexyl-2-methylbenzo[d]thiazole-6-sulfonamide
Rendimiento 97.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    LavadoThe reaction mixture was then washed with water (2×, 50 ml) and brine (1×, 50 ml)
  2. 2
    SecadoThe organic layer was then dried with sodium sulfate
  3. 3
    Otroevaporated
  4. 4
    OtroThe residue thus obtained
  5. 5
    OtroThe white solid that precipitated
  6. 6
    Filtraciónwas filtered
  7. 7
    Otrothe filtrate evaporated to dryness

Procedimiento

A solution of Compound 2 (5.0 g, 20.2 mmol) from step (b) of Example 1 dissolved in chloroform (30 ml) was added drop wise to a solution of dihexylamine (4.5 g, 24.2 mmol) in chloroform (20 ml). The combined mixture was stirred at room temperature for 2 hours. The reaction mixture was then washed with water (2×, 50 ml) and brine (1×, 50 ml). The organic layer was then dried with sodium sulfate and evaporated. The residue thus obtained was suspended in ca. 5 ml hot ethyl acetate and this solution was then slowly added to 40 ml hexane. The white solid that precipitated was filtered and the filtrate evaporated to dryness to provide 7.76 g (97%) of Compound 20 as a syrupy liquid, Rf=0.43 (30% ethyl acetate in hexane). The structure of this compound is given below:

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08574881B2uspto-grants-2013_11