Reaction #640545

ord-e185e36aa8fb4072a8c54108070b839b

Reaction equation

CCOC(C)=O
ethyl acetate
Cc1c(O)cccc1C(=O)O
3-hydroxy-2-methylbenzoic acid
On1nnc2ccccc21
N-hydroxybenzotriazole
ClCCCl
EDC
NC(=O)c1ccccc1
benzamide
Yield 183.0%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.WAITAfter 15 hours at room temperature
  2. 2
    Washwashed with 5% citric acid, saturated sodium bicarbonate, brine
  3. 3
    Otherdried
  4. 4
    Filtrationfiltered
  5. 5
    Concentrationconcentrated
  6. 6
    Otherto afford 590 mg of crude material
  7. 7
    OtherThis was chromatographed on silica gel using 50-80% ethyl acetate/methylene chloride as eluent

Procedure

To a solution of 175 mg (1.15 mmol) of 3-hydroxy-2-methylbenzoic acid and 203 mg (1.5 mmol) of N-hydroxybenzotriazole in 6 mL of anhydrous N,N-dimethylformamide at 0° C., was added 220 mg (1.15 mmol) of EDC. After 20 minutes of activation at 0° C. and 1 hour at room temperature, 392 mg (1.0 mmol) of 2R-hydroxy-3-[(2-methylpropyl)(4-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 590 mg of crude material. This was chromatographed on silica gel using 50-80% ethyl acetate/methylene chloride as eluent to afford 255 mg of pure benzamide, N-[2R-hydroxy-3-[[(4-aminophenyl)sulfonyl](2-methylpropyl)amino]-1S-(phenylmethyl)propyl]-3-hydroxy-2-methyl, m/e=526(M+H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE042889E1uspto-grants-2011_11