Trifluoroacetic acid → N-((2R)-2-methylamino-3-phenylpropyl)methansulfonamide

HRID 495834Notes

Reaction equation

HRID 495834 reaction equation
FC(F)(F)C(O)=O.C(O[C:13](=O)[N:14]([C@H:16]([CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[CH2:17][NH:18][S:19]([CH3:22])(=[O:21])=[O:20])C)(C)(C)C>ClCCl>[CH3:13][NH:14][C@H:16]([CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[CH2:17][NH:18][S:19]([CH3:22])(=[O:20])=[O:21]

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 54199950N-((1R)-1-Benzyl-2-((methylsulfonyl)amino)ethyl)-N-methylcarbamic acid tert-butylester

Product 1

HCID 54473398N-((2R)-2-methylamino-3-phenylpropyl)methansulfonamideYield 101.7%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Conditions

Temperature
0 °C

Procedure

At 0° C., trifluoroacetic acid (5 ml) was added to a solution of N-((1R)-1-benzyl-2-((methylsulfonyl)amino)ethyl)-N-methylcarbamic acid tert-butylester (913 mg, 2.67 mmol) in dichloromethane (5 ml). The reaction mixture was stirred for 15 min at 0° C. The solvent was removed in vacuo without warming. The residue was dissolved in dichloromethane (50 ml) and the solvent was removed in vacuo. The latter procedure was repeated two times. The crude product was purified by flash chromatography on silica (20 g), using dichloromethane/methanol/25% aqueous ammonia as eluent, to give 658 mg of N-((2R)-2-methylamino-3-phenylpropyl)methansulfonamide.

Workup

  1. customThe solvent was removed in vacuo
  2. temperaturewithout warming
  3. dissolutionThe residue was dissolved in dichloromethane (50 ml)
  4. customthe solvent was removed in vacuo
  5. customThe crude product was purified by flash chromatography on silica (20 g)

Sources & evidence

ORD record
ord-a3e5762f5c7a40a5b440ca618a1ef12c
Source dataset
uspto-grants-2005_09
Patent number
US06939880B2

Reaction notes

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