1-(2-Methylsulfanyl-ethyl)-3,4-dihydro-isoquinoline-3-carboxylic acid methyl ester → 1-(2-Methylsulfanyl-ethyl)-isoquinoline-3-carboxylic acid methyl ester

HRID 1910171Notes

Reaction equation

HRID 1910171 reaction equation
[CH3:1][O:2][C:3]([CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:7]([CH2:15][CH2:16][S:17][CH3:18])=[N:6]1)=[O:4]>ClCCl.C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[CH3:1][O:2][C:3]([C:5]1[N:6]=[C:7]([CH2:15][CH2:16][S:17][CH3:18])[C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:4]

Participants

4

Procedure

1.297 g (7 mmol) of copper acetate was added to a solution of 923 mg (3.5 mmol) of 1-(2-methylsulfanyl-ethyl)-3,4-dihydro-isoquinoline-3-carboxylic acid methyl ester in 10 mL of dichloromethane, stirring at room temperature overnight. This reaction mixture was concentrated and purified by column chromatography on silica gel to give 266 mg (29%) of 1-(2-methylsulfanyl-ethyl)-isoquinoline-3-carboxylic acid methyl ester. LCMS: 262 (M+1)+.

Workup

  1. concentrationThis reaction mixture was concentrated
  2. custompurified by column chromatography on silica gel

Sources & evidence

ORD record
ord-e674eff2a3c64c84937cffd282a25929
Source dataset
uspto-grants-2013_12
Patent number
US08598353B2

Reaction notes

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