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

HRID 1367900Notes

Reaction equation

HRID 1367900 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-ac412dc8c88741fc8e68ad3ac3003686
Source dataset
uspto-grants-2011_02
Patent number
US07893267B2

Reaction notes

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