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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Isoquinolin-3-Amine → 5,6,7,8-Tetrahydroisoquinolin-3-amine

HRID 1740970
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HRID 1740970 반응식
[NH2:1][C:2]1[N:3]=[CH:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2.[H][H]>FC(F)(F)C(O)=O.[Pt]=O>[NH2:1][C:2]1[N:3]=[CH:4][C:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C:10]=2[CH:11]=1
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참가 물질

5

반응물 2

HCID 311869Isoquinolin-3-AmineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 133023975,6,7,8-Tetrahydroisoquinolin-3-amine수율 34%

시약·촉매·용매 2

HCID 82844Platinum oxide (PtO)촉매HCID 6422Trifluoroacetic acid용매

실험 절차

Using the method of Example 63, Step A, 75 mg of 3-aminoisoquinoline (7.73 mmoles) and 8.7 mg platinum oxide in 2 mL of trifluoroacetic acid was shaken under 40 psi of hydrogen for 3 h. The mixture was filtered and catalyst was washed with ethyl acetate. After concentrating the filtrate, the residue was dissolved in 10 mL of ethyl acetate and washed with 5 mL of saturated aquous sodium bicarbonate. The organic solution was dried (sodium sulfate), decanted, and concentrated to give a yellow syrup. Flash coumn chromatography on 19 g of silica gel, eluting with 600 mL of 50% ethyl acetate/hexane gave 26.5 mg (34% yield) of 3-amino-5,6,7,8-tetrahydroisoquinoline as a pale yellow solid.

후처리

  1. filtrationThe mixture was filtered
  2. washcatalyst was washed with ethyl acetate
  3. concentrationAfter concentrating the filtrate
  4. dissolutionthe residue was dissolved in 10 mL of ethyl acetate
  5. washwashed with 5 mL of saturated aquous sodium bicarbonate
  6. dry with materialThe organic solution was dried (sodium sulfate)
  7. customdecanted
  8. concentrationconcentrated
  9. customto give a yellow syrup
  10. washFlash coumn chromatography on 19 g of silica gel, eluting with 600 mL of 50% ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-590e9480a04b43cd8fc401785bc627d0
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05972975

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