Methylamine → Benzyl N-[(1S)-1-(methylcarbamoyl)-2-phenylethyl]carbamate

HRID 2399919Notes

Reaction equation

HRID 2399919 reaction equation
[N+](C1C=CC(O[C:11](=[O:31])[C@H:12]([CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[NH:13][C:14]([O:16][CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[O:15])=CC=1)([O-])=O.[CH3:32][NH2:33]>C(Cl)Cl.C(O)C>[CH3:32][NH:33][C:11](=[O:31])[C@H:12]([CH2:24][C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1)[NH:13][C:14]([O:16][CH2:17][C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1)=[O:15]

Participants

5

Reactant 2

HCID 6329MethylamineHCID 151025Z-Phe-ONp

Product 1

HCID 13443905Benzyl N-[(1S)-1-(methylcarbamoyl)-2-phenylethyl]carbamateYield 81%

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 6344DichloromethaneSolvent2×

Procedure

To a stirred solution of N-benzyloxycarbonyl-L-phenylalanine p-nitrophenylester (5.0 g, 11.9 mmol) in DCM at 0° C. was slowly added a solution of 8M methylamine (1.5 ml, 11.9 mmol) in ethanol. The reaction immediately turned bright yellow and was stirred for 0.5 h. The reaction was diluted with DCM (50 ml), washed with 10% sodium carbonate (1×50 ml), brine (2×50 ml) and dried over anhydrous magnesium sulphate. Filtration and evaporation gave a white residue which was crystallised from ethyl acetate/hexane to give N-benzyloxycarbonyl-L-phenylalanine methylamide (3.0 g, 81%) as a white crystalline solid.

Workup

  1. customThe reaction immediately turned bright yellow
  2. washwashed with 10% sodium carbonate (1×50 ml), brine (2×50 ml)
  3. dry with materialdried over anhydrous magnesium sulphate
  4. filtrationFiltration and evaporation
  5. customgave a white residue which
  6. customwas crystallised from ethyl acetate/hexane

Sources & evidence

ORD record
ord-02e30017e87445bc882fa18a8f6b8832
Source dataset
uspto-grants-1995_09
Patent number
US05451676

Reaction notes

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