Sodium Methoxide → 1-ethoxycarbonylmethyl-3-(1-ethoxycarbonyl-3-phenylpropylamino)-2,3,4,5-tetrahydro-1H-[1]benzazepine-2-one

HRID 647881Notes

Reaction equation

HRID 647881 reaction equation
[CH2:1]([O:3][C:4]([CH:6]([NH:15][CH:16]([CH2:22][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=1[NH:30][CH2:31][C:32]([O:34][CH2:35][CH3:36])=[O:33])[C:17](OCC)=[O:18])[CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:5])[CH3:2].C[O-].[Na+]>CO>[CH2:35]([O:34][C:32]([CH2:31][N:30]1[C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][C:24]=2[CH2:23][CH2:22][CH:16]([NH:15][CH:6]([C:4]([O:3][CH2:1][CH3:2])=[O:5])[CH2:7][CH2:8][C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[C:17]1=[O:18])=[O:33])[CH3:36]

Participants

4

Reactant 2

HCID 10942334Sodium MethoxideHCID 53634656Ethyl 2-(1-ethoxycarbonyl-3-phenylpropylamino)-4-[o-(ethoxycarbonylmethylamino)phenyl]butyrate

Product 1

HCID 132435171-ethoxycarbonylmethyl-3-(1-ethoxycarbonyl-3-phenylpropylamino)-2,3,4,5-tetrahydro-1H-[1]benzazepine-2-one

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent2×

Procedure

A solution of ethyl 2-(1-ethoxycarbonyl-3-phenylpropylamino)-4-[o-(ethoxycarbonylmethylamino)phenyl]butyrate (5.6 g) in methanol (100 ml) is added to a solution of sodium methoxide in methanol [prepared from sodium (0.25 g) and methanol (50 ml)] with stirring under a nitrogen atmosphere. The reaction mixture is refluxed for 65 hours, then evaporated under reduced pressure. The residue is distributed between water (50 ml) and dichloromethane (200 ml). The aqueous solution is extracted with dichloromethane (200 ml) and the combined organic solutions washed with water (50 ml) and dried over potassium carbonate. Evaporation of the solvent gives as a mixture of isomers A and B of 1-ethoxycarbonylmethyl-3-(1-ethoxycarbonyl-3-phenylpropylamino)-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one, which is separated by chromatography on silica gel and converted to the individual maleate salts as described in example 10.

Workup

  1. temperatureThe reaction mixture is refluxed for 65 hours
  2. customevaporated under reduced pressure
  3. extractionThe aqueous solution is extracted with dichloromethane (200 ml)
  4. washthe combined organic solutions washed with water (50 ml)
  5. dry with materialdried over potassium carbonate
  6. customEvaporation of the solvent

Sources & evidence

ORD record
ord-69fb12a5f30047afb375600abd0388c2
Source dataset
uspto-grants-1983_10
Patent number
US04410520

Reaction notes

Loading…