Triethylamine → Benzamide

HRID 491383Notes

Reaction equation

HRID 491383 reaction equation
C([N:3](CC)CC)C.[C:8]1(C)[C:9]([C:14](Cl)=[O:15])=[CH:10][CH:11]=[CH:12][CH:13]=1.C(OCC)(=O)C>C(Cl)Cl>[C:14]([NH2:3])(=[O:15])[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:8]=1

Participants

5

Procedure

To a solution of 391 mg (1 mmol) of 2R-hydroxy-3-[(2-methylpropyl)(4-aminophenyl)sulfonyl]amino-1S-(phenylmethyl)propylamine in 3 mL of anhydrous methylene chloride, was added 0.42 mL (3 mmol) of triethylamine, then at room temperature, 0.12 mL (0.9 mmol) of orthotoluoyl chloride was added. After 15 hours at room temp ethyl acetate was added, washed with 5%. citric acid, saturated sodium bicarbonate, brine, dried, filtered and concentrated to afford 420 mg of crude material. This was chromatographed on 40 g of silica gel using 50% ethyl acetate/hexane to afford 368 mg of pure benzamide, N-[2R-hydroxy-3-[[(4-aminophenyl)sulfonyl](2-methylpropyl)amino]-1S-(phenylmethyl)propyl]-2-methyl, m/e=516 (M+Li).

Workup

  1. washwashed with 5%
  2. dry with materialcitric acid, saturated sodium bicarbonate, brine, dried
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customto afford 420 mg of crude material
  6. customThis was chromatographed on 40 g of silica gel using 50% ethyl acetate/hexane

Sources & evidence

ORD record
ord-d4f10a00094642a981400eaa0091faf4
Source dataset
uspto-grants-2009_05
Patent number
US07531538B2

Reaction notes

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