Reacción #640546

ord-039d883448e74fe3a24168f0cc445e0f

Ecuación de reacción

CCOC(C)=O
ethyl acetate
Cc1c(O)cccc1C(=O)O
3-hydroxy-2-methylbenzoic acid
On1nnc2ccccc21
N-hydroxybenzotriazole
ClCCCl
EDC
NC(=O)c1ccccc1
benzamide

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.WAITAfter 15 hours at room temperature
  2. 2
    Lavadowashed with 5% citric acid, saturated sodium bicarbonate, brine
  3. 3
    Otrodried
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated
  6. 6
    Otroto afford 330 mg of crude material
  7. 7
    OtroThis was chromatographed on silica gel using 30-70% ethyl acetate/methylene chloride as eluent

Procedimiento

To a solution of 134 mg (0.88 mmol) of 3-hydroxy-2-methylbenzoic acid and 155 mg (1.15 mmol) of N-hydroxybenzotriazole in 5 mL of anhydrous N,N-dimethylformamide at 0° C., was added 167 mg (0.88 mmol) of EDC. After 20 minutes of activation at 0° C. and 1 hour at room temperature, 300 mg (1.0 mmol) of 2R-hydroxy-3-[(2-methylpropyl)(3-aminophenyl)sulfonyl]amino-1S-(phenylmethyl)propylamine was added. After 15 hours at room temperature, ethyl acetate was added, washed with 5% citric acid, saturated sodium bicarbonate, brine, dried, filtered and concentrated to afford 330 mg of crude material. This was chromatographed on silica gel using 30-70% ethyl acetate/methylene chloride as eluent to afford 230 mg of pure benzamide, N-[2R-hydroxy-3-[[(3-aminophenyl)sulfonyl](2-methylpropyl)amino]-1S-(phenylmethyl)propyl]-3-hydroxy-2-methyl.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE042889E1uspto-grants-2011_11