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

반응식

HRID 35736 반응식
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

참가 물질

4

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-cf603f7c39f9432da68b883f88430369
출처 데이터셋
uspto-grants-1988_08
특허 번호
US04767862

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