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Ethyl 3,4-dihydro-6,7-dimethoxy-1-isoquinolinecarboxylate → HCID 20202902, compound

HRID 1367886
Notes
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Reaction equation

HRID 1367886 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:15]2[C:10](=[CH:11][C:12]([O:18][CH3:19])=[C:13]([O:16][CH3:17])[CH:14]=2)[CH2:9][CH2:8][N:7]=1)=[O:5])[CH3:2]>[Pd]>[CH2:1]([O:3][C:4]([C:6]1[C:15]2[C:10](=[CH:11][C:12]([O:18][CH3:19])=[C:13]([O:16][CH3:17])[CH:14]=2)[CH:9]=[CH:8][N:7]=1)=[O:5])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 4060727Ethyl 3,4-dihydro-6,7-dimethoxy-1-isoquinolinecarboxylate

Product 1

HCID 20202902HCID 20202902, compoundYield 98%

Reagents, catalysts & solvents 1

HCID 23938PalladiumCatalyst

Procedure

To a refluxing solution of 2.0 g (8.0 mmol) of 6,7-dimethoxy-3,4-dihydro-isoquinoline-1-carboxylic acid ethyl ester was added to 2.0 g of 10% Pd—C. After 12 h at reflux, the reaction mixture was cooled, filtered through celite, and evaporated under reduced pressure to provide 2.0 g (98%) of 6,7-dimethoxy-isoquinoline-1-carboxylic acid ethyl ester. LCMS: 262 (M+1)+.

Workup

  1. temperatureAfter 12 h at reflux
  2. temperature
the reaction mixture was cooled
  • filtrationfiltered through celite
  • customevaporated under reduced pressure
  • Sources & evidence

    ORD record
    ord-2ff5c155db1c4ba0bc420650191d1c83
    Source dataset
    uspto-grants-2011_02
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07893267B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes