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Water → 6,7-Dimethoxy-2-(piperidin-4-ylmethyl)-1,2,3,4-tetrahydroisoquinoline

HRID 1393030
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HRID 1393030 반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].[CH3:7][O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][C:18]=1[O:19][CH3:20])[CH2:15][N:14]([C:21]([CH:23]1[CH2:28][CH2:27][NH:26][CH2:25][CH2:24]1)=O)[CH2:13][CH2:12]2.O.[OH-].[Na+]>O1CCCC1>[CH3:7][O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][C:18]=1[O:19][CH3:20])[CH2:15][N:14]([CH2:21][CH:23]1[CH2:28][CH2:27][NH:26][CH2:25][CH2:24]1)[CH2:13][CH2:12]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 14798Sodium HydroxideHCID 21226445Aluminium lithium hydrideHCID 23133306HCID 23133306, 화합물

생성물 1

HCID 231333026,7-Dimethoxy-2-(piperidin-4-ylmethyl)-1,2,3,4-tetrahydroisoquinoline

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A 1 M solution of LiAlH4 in dry tetrahydrofuran (12 ml) was added dropwise to a solution of (6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)(piperidin-4-yl)methanone (2 g, 6.6 mmol) in dry tetrahydrofuran (60 ml) under argon atmosphere. The mixture was refluxed overnight. Water was added to the crude, made alkaline with 1 N NaOH and the salts formed was filtered over celite. Extraction with ethyl acetate yielded a solution that was dried with Na2SO4 and concentrated in vacuo to give and oil that was purified by flash chromatography.

후처리

  1. temperatureThe mixture was refluxed overnight
  2. customthe salts formed
  3. filtrationwas filtered over celite
  4. extractionExtraction with ethyl acetate
  5. customyielded a solution that
  6. dry with materialwas dried with Na2SO4
  7. concentrationconcentrated in vacuo
  8. customto give
  9. customoil that was purified by flash chromatography

출처 및 근거

ORD 기록
ord-5b8612223c60439db6fad2af60eb7619
출처 데이터셋
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07345057B2

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