Water → HCID 67147907, compound

HRID 2426342Notes

Reaction equation

HRID 2426342 reaction equation
[CH2:1]([NH2:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].[CH2:9]([O:11][C@@H:12]([CH2:17][C:18]1[CH:19]=[N:20][C:21]([C:24]2[CH:29]=[CH:28][CH:27]=[C:26]([N:30]([CH3:43])[C:31](OC3C=CC([N+]([O-])=O)=CC=3)=[O:32])[CH:25]=2)=[CH:22][CH:23]=1)[C:13]([O:15][CH3:16])=[O:14])[CH3:10].O>CN(C)C=O>[CH2:9]([O:11][C@@H:12]([CH2:17][C:18]1[CH:19]=[N:20][C:21]([C:24]2[CH:29]=[CH:28][CH:27]=[C:26]([N:30]([CH3:43])[C:31]([NH:8][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7])=[O:32])[CH:25]=2)=[CH:22][CH:23]=1)[C:13]([O:15][CH3:16])=[O:14])[CH3:10]

Participants

5

Reactant 3

HCID 962WaterHCID 81271-HeptanamineHCID 67147910HCID 67147910, compound

Product 1

HCID 67147907HCID 67147907, compoundYield 50%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
80 °C

Procedure

70 μl (0.45 mmol) of heptylamine are added to a solution of 110 mg (0.25 mmol) of methyl 2(S)-ethoxy-3-(6-{3-[methyl(4-nitrophenoxycarbonyl)amino]phenyl}pyrid-3-yl)propanoate in 3 ml of dimethylformamide. The reaction medium is heated at 80° C. for 3 hours. After addition of water, the reaction medium is extracted with ethyl acetate. The organic phase is dried over magnesium sulfate, filtered and evaporated. The residue obtained is purified by thin-layer chromatography on silica eluted with a 6/4 and then 5/5 heptane/ethyl acetate mixture. 50 mg (50%) of methyl 2(S)-ethoxy-3-{6-[3-(3-heptyl-1-methylureido)phenyl]pyrid-3-yl}propanoate are obtained.

Workup

  1. extractionthe reaction medium is extracted with ethyl acetate
  2. dry with materialThe organic phase is dried over magnesium sulfate
  3. filtrationfiltered
  4. customevaporated
  5. customThe residue obtained
  6. customis purified by thin-layer chromatography on silica
  7. washeluted with a 6/4

Sources & evidence

ORD record
ord-1b35a40c7b554fedb948d815682b40c1
Source dataset
uspto-grants-2011_06
Patent number
US07968560B2

Reaction notes

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