Fumaric Acid → HCID 178439975, compound

HRID 21879Notes

Reaction equation

HRID 21879 reaction equation
[CH2:1]([N:3]1[CH2:8][CH2:7][C:6]2[N:9]=[C:10]([CH2:49][CH2:50][CH3:51])[N:11]([CH2:12][C:13]3[CH:18]=[CH:17][C:16]([C:19]4[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=4[C:25]4[N:29](C(C5C=CC=CC=5)(C5C=CC=CC=5)C5C=CC=CC=5)[N:28]=[N:27][N:26]=4)=[CH:15][CH:14]=3)[C:5]=2[CH:4]1[C:52]([O:54][CH2:55][CH3:56])=[O:53])[CH3:2].C(O)(=O)/C=C/C(O)=O>C(O)C>[CH2:1]([N:3]1[CH2:8][CH2:7][C:6]2[N:9]=[C:10]([CH2:49][CH2:50][CH3:51])[N:11]([CH2:12][C:13]3[CH:18]=[CH:17][C:16]([C:19]4[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=4[C:25]4[NH:29][N:28]=[N:27][N:26]=4)=[CH:15][CH:14]=3)[C:5]=2[CH:4]1[C:52]([O:54][CH2:55][CH3:56])=[O:53])[CH3:2]

Participants

4

Procedure

A mixture of ethyl 5-ethyl-2-n-propyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate (1.10 g), fumaric acid (1.2 g) ane ethanol (20 ml) is refluxed for one hour. The mixture is evaporated, and the residue is dissolved in chloroform, and the mixture is washed with a saturated sodium hydrogen carbonate solution and brine, dried and evaporated. The residue is purified by silica gel column chromatography (solvent; chloroform/methanol) to give ethyl 5-ethyl-2-n-propyl-3-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate (0.65 g) as a white foam.

Workup

  1. temperatureis refluxed for one hour
  2. customThe mixture is evaporated
  3. dissolutionthe residue is dissolved in chloroform
  4. washthe mixture is washed with a saturated sodium hydrogen carbonate solution and brine
  5. customdried
  6. customevaporated
  7. customThe residue is purified by silica gel column chromatography (solvent; chloroform/methanol)

Sources & evidence

ORD record
ord-fe99ccd86c0a41f48e535812ac871046
Source dataset
uspto-grants-1995_06
Patent number
US05424316

Reaction notes

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