2-Benzoyl-1-(3,4,5-trimethoxybenzyl)-6,7-dichloro-1-cyano-1,2-dihydroisoquinoline → 6,7-Dichloro-1-(3,4,5-trimethyoxybenzyl)isoquinoline hydrochloride

HRID 35736

Reaktionsgleichung

Reaktionsgleichung von HRID 35736
C([N:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][C:13]([Cl:20])=[C:14]([Cl:19])[CH:15]=2)[C:10]1([CH2:23][C:24]1[CH:29]=[C:28]([O:30][CH3:31])[C:27]([O:32][CH3:33])=[C:26]([O:34][CH3:35])[CH:25]=1)C#N)(=O)C1C=CC=CC=1>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1.C1(C)C=CC=CC=1>[ClH:19].[Cl:19][C:14]1[CH:15]=[C:16]2[C:11](=[CH:12][C:13]=1[Cl:20])[C:10]([CH2:23][C:24]1[CH:25]=[C:26]([O:34][CH3:35])[C:27]([O:32][CH3:33])=[C:28]([O:30][CH3:31])[CH:29]=1)=[N:9][CH:18]=[CH:17]2

Komponenten

4

Edukt 1

HCID 136795072-Benzoyl-1-(3,4,5-trimethoxybenzyl)-6,7-dichloro-1-cyano-1,2-dihydroisoquinoline

Produkt 1

HCID 212949006,7-Dichloro-1-(3,4,5-trimethyoxybenzyl)isoquinoline hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 66133Benzyl triethylammonium chlorideKatalysatorHCID 1140TolueneLösungsmittel

Versuchsvorschrift

Benzyltriethylammonium chloride (0.118 g, 0.517 mmole) was added to a solution of 2.3 g (4.5 mmole) of 2-benzoyl-1-(3,4,5-trimethoxybenzyl)-6,7-dichloro-1-cyano-1,2-dihydroisoquinoline in 40 ml of toluene. The stirred solution was flushed with nitrogen and then 19 ml of 50% sodium hydroxide solution was added in one portion. The reaction mixture was stirred and refluxed under nitrogen for 1.5 hours; it was then cooled and 25 ml of water and 25 ml of ethyl acetate were added. The organic layer was separated, washed (water, brine), dried (magnesium sulfate) and concentrated. The residue in a small volume of methanol was acidified with hydrogen chloride and ether was added to give 6,7-dichloro-1-(3,4,5-trimethyoxybenzyl)isoquinoline hydrochloride as white crystals, melting at 211°-212° C., after recrystallization from methanol-ether.

Aufarbeitung

  1. customThe stirred solution was flushed with nitrogen
  2. addition19 ml of 50% sodium hydroxide solution was added in one portion
  3. temperaturerefluxed under nitrogen for 1.5 hours
  4. temperatureit was then cooled
  5. addition25 ml of water and 25 ml of ethyl acetate were added
  6. customThe organic layer was separated
  7. washwashed (water, brine)
  8. dry with materialdried (magnesium sulfate)
  9. concentrationconcentrated
  10. additionwas added

Quellen und Nachweise

ORD-Eintrag
ord-cf603f7c39f9432da68b883f88430369
Quelldatensatz
uspto-grants-1988_08
Patentnummer
US04767862

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