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Sodium Hydroxide → 3-[2-(N,N-Dimethylamino)ethyl]-1,2,3,4-tetrahydroquinoline

HRID 2269714
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HRID 2269714 반응식
[CH3:1][N:2]([CH3:17])[C:3](=O)[CH2:4][CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][C:6]1=O.[OH-].[Na+]>Cl>[CH3:1][N:2]([CH2:3][CH2:4][CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH2:6]1)[CH3:17]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 10585665N,N-Dimethyl-2-oxo-1,2,3,4-tetrahydro-3-quinolineacetoamide

생성물 1

HCID 183331263-[2-(N,N-Dimethylamino)ethyl]-1,2,3,4-tetrahydroquinoline수율 75.1%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

Borane-THF complex (1M; 15 ml) was added to N,N-dimethyl-2-oxo-1,2,3,4-tetrahydro-3-quinolineacetoamide (590 mg), which was heated under reflux for 3.5 hours. 6N hydrochloric acid (10 ml) was added to the reaction mixture, which was heated under reflux overnight. 6N sodium hydroxide was added to the reaction mixture to adjust pH to 7 and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution, then dried and concentrated. The residue was purified by alumina column chromatography (eluent: hexane/ethyl acetate=1/1) to obtain the entitled compound (390 mg) as an oily substance.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 3.5 hours
  3. temperaturewas heated
  4. temperatureunder reflux overnight
  5. extractionextracted with ethyl acetate
  6. washThe organic layer was washed with a saturated aqueous sodium bicarbonate solution
  7. dry with materiala saturated aqueous sodium chloride solution, then dried
  8. concentrationconcentrated
  9. customThe residue was purified by alumina column chromatography (eluent: hexane/ethyl acetate=1/1)

출처 및 근거

ORD 기록
ord-5e6b2901d14c47e4aba22c49b92f3992
출처 데이터셋
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06329389B1

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