Ethanol → HCID 178442133, compound

HRID 2210413Notes

Reaction equation

HRID 2210413 reaction equation
[CH2:1]([C:6]1[CH:31]=[CH:30][C:9]([CH:10]=[CH:11][C:12]([NH:14][C:15]2[C:20]3[O:21][CH:22]([C:25]4[NH:29][N:28]=[N:27][N:26]=4)[CH2:23][O:24][C:19]=3[CH:18]=[CH:17][CH:16]=2)=[O:13])=[CH:8][CH:7]=1)[CH2:2][CH2:3][CH2:4][CH3:5].CO.C(O)C.[H][H]>[C].[Pd].C(OCC)(=O)C>[CH2:1]([C:6]1[CH:31]=[CH:30][C:9]([CH2:10][CH2:11][C:12]([NH:14][C:15]2[C:20]3[O:21][CH:22]([C:25]4[NH:29][N:28]=[N:27][N:26]=4)[CH2:23][O:24][C:19]=3[CH:18]=[CH:17][CH:16]=2)=[O:13])=[CH:8][CH:7]=1)[CH2:2][CH2:3][CH2:4][CH3:5]

Participants

7

Reactant 4

HCID 702EthanolHCID 887MethanolHCID 178418361HCID 178418361, compoundHCID 178442132HCID 178442132, compound

Product 1

HCID 178442133HCID 178442133, compoundYield 93.1%

Reagents, catalysts & solvents 2

HCID 178418390HCID 178418390, compoundCatalystHCID 8857Ethyl AcetateSolvent

Procedure

8- (p-pentylcinnamoyl) amino-2- (5-tetrazolyl) -1,4-benzodioxane (216 mg; synthesized in example 2(1)) and palladium-carbon (50 mg; content 5%) were suspended in a mixed solvent (6 ml) of methanol, ethanol and ethyl acetate (1:1:1). In an atmosphere of hydrogen, the suspension was stirred for 90 min at room temperature. After stirring, the suspension was filtered through celite. The filtrate was condensed under reduced pressure. The residue was purified by column chromatography on silica gel (methylene chloride: methanol=19:1) to give the title compound (202 mg) having the following physical data:

Workup

  1. filtrationthe suspension was filtered through celite
  2. customcondensed under reduced pressure
  3. customThe residue was purified by column chromatography on silica gel (methylene chloride: methanol=19:1)

Sources & evidence

ORD record
ord-094cf2531c044952bd1170bc3e036089
Source dataset
uspto-grants-1995_10
Patent number
US05459134

Reaction notes

Loading…