Dimethylformamide → HCID 22912858, compound

HRID 1378737Notes

Reaction equation

HRID 1378737 reaction equation
[Cl:1][C:2]1[C:7]([NH:8][C:9]([CH3:14])([C:11]([OH:13])=[O:12])[CH3:10])=[C:6]([N+:15]([O-:17])=[O:16])[CH:5]=[CH:4][CH:3]=1.[CH3:18]N(C=O)C.C(=O)([O-])[O-].[K+].[K+].IC>O>[CH3:18][O:12][C:11](=[O:13])[C:9]([CH3:10])([CH3:14])[NH:8][C:7]1[C:2]([Cl:1])=[CH:3][CH:4]=[CH:5][C:6]=1[N+:15]([O-:17])=[O:16]

Participants

6

Reactant 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 22912940HCID 22912940, compound

Product 1

HCID 22912858HCID 22912858, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A mixture of N-(6-chloro-2-nitrophenyl)-2-methylalanine (X, EXAMPLE 14, 11.4 g), DMF (130 ml), potassium carbonate (18.2 g) and iodomethane (13.8 ml) is stirred at 20°-25° for 16 hr, diluted with water, extracted several times with ether. The ether phases are combined and are washed with water and saline, dried over magnesium sulfate and concentrated to give the title compound, IR (mineral oil) 3369, 2990, 2951, 1738, 1598, 1534, 1492, 1451, 1386, 1337, 1277, 1188, 1145, 1103 and 749 cm-1 ; NMR (CDCl3) 7.97, 7.55, 6.94, 6.89, 3.78 and 1.53 δ; MS (m/z) 272 and 213.

Workup

  1. extractionextracted several times with ether
  2. washare washed with water and saline
  3. dry with materialdried over magnesium sulfate
  4. concentrationconcentrated

Sources & evidence

ORD record
ord-50fd4ee945484f76bb2516a17d2fd29f
Source dataset
uspto-grants-1997_09
Patent number
US05668282

Reaction notes

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