1,2-Dimethoxyethane → N-Decyl-3-(3-[4-Methoxycarbonyl-2-oxo-pyrrolidino]phenyl)propenamide

HRID 66797Notes

Reaction equation

HRID 66797 reaction equation
[CH2:1]([NH:11][C:12](=[O:30])[CH:13]=[CH:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([N:21]2[CH2:25][CH:24]([C:26]([OH:28])=[O:27])[CH2:23][C:22]2=[O:29])[CH:16]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[CH3:31]OCCOC.[N+](=C)=[N-]>C(O)(=O)C.CCOCC>[CH2:1]([NH:11][C:12](=[O:30])[CH:13]=[CH:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([N:21]2[CH2:25][CH:24]([C:26]([O:28][CH3:31])=[O:27])[CH2:23][C:22]2=[O:29])[CH:16]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]

Participants

6

Reactant 3

HCID 80711,2-DimethoxyethaneHCID 9550Diazomethane2×HCID 53878346N-Decyl-3-[3-(4-carboxy-2-oxo-pyrrolidino)phenyl]propenamide

Product 1

HCID 53968862N-Decyl-3-(3-[4-Methoxycarbonyl-2-oxo-pyrrolidino]phenyl)propenamide

Reagents, catalysts & solvents 2

HCID 176Acetic AcidCatalystHCID 3283Diethyl EtherSolvent

Procedure

To a stirred mixture of 415 mg. of N-decyl-3-(3-[4-carboxy-2-oxo-pyrrolidino]phenyl)propenamide and 15 ml. of 1,2-dimethoxyethane is added a solution of 1.5 mmoles of diazomethane in 5 ml. of ether. The reaction mixture is stirred at room temperature for 16 hours, and then the excess diazomethane is decomposed by the addition of a few drops of acetic acid. The total solvents are removed by evaporation in vacuo, and the residue is dissolved in ethyl acetate. The ethyl acetate solution is washed with 1 N sodium hydroxide, followed by water, followed by saturated sodium chloride solution, and then dried using sodium sulfate. Evaporation of the dried ethyl acetate solution in vacuo affords the title compound.

Workup

  1. additionTo a stirred mixture of 415 mg
  2. customThe total solvents are removed by evaporation in vacuo
  3. dissolutionthe residue is dissolved in ethyl acetate
  4. washThe ethyl acetate solution is washed with 1 N sodium hydroxide
  5. customdried
  6. customEvaporation of the dried ethyl acetate solution in vacuo

Sources & evidence

ORD record
ord-7c295665dd2b46f7a2431202d095780c
Source dataset
uspto-grants-1982_08
Patent number
US04343813

Reaction notes

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