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Formaldehyde → 1-[(4-Aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)methyl]pyrrolidin-3-ol

HRID 578757
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HRID 578757 반응식
[NH:1]1[CH2:5][CH2:4][CH:3]([OH:6])[CH2:2]1.[CH2:7]=O.[N:9]1[N:10]2[CH:18]=[CH:17][CH:16]=[C:11]2[C:12]([NH2:15])=[N:13][CH:14]=1>C(O)(=O)C>[NH2:15][C:12]1[C:11]2=[CH:16][CH:17]=[C:18]([CH2:7][N:1]3[CH2:5][CH2:4][CH:3]([OH:6])[CH2:2]3)[N:10]2[N:9]=[CH:14][N:13]=1
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참가 물질

5

반응물 3

HCID 712FormaldehydeHCID 982104-HydroxypyrrolidineHCID 10441749Pyrrolo[2,1-f][1,2,4]triazin-4-amine

생성물 1

HCID 903891581-[(4-Aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)methyl]pyrrolidin-3-ol

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

실험 절차

3-Pyrrolidinol (1.56 g, 17.9 mmol) and 37% formalin solution (1.45 g, 17.9 mmol) were dissolved in acetic acid (75 mL) and stirred at room temperature for 10 min. To this solution was added a solution of pyrrolo[2,1-f][1,2,4]triazin-4-amine (2.0 g, 14.9 mmol) in acetic acid (75 mL), and the mixture was stirred at 60° C. for 4 h. After evaporation, the residue was taken up in 200 mL of 1 N aqueous potassium carbonate solution and extracted with ethyl acetate (3×200 mL). The combined organic layers were washed with brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by preparative HPLC (method 4) to give 390 mg (11% of th.) of the title compound.

후처리

  1. stirringthe mixture was stirred at 60° C. for 4 h
  2. customAfter evaporation
  3. extractionextracted with ethyl acetate (3×200 mL)
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by preparative HPLC (method 4)

출처 및 근거

ORD 기록
ord-8d3bb599ecce4a5ea8e7598b1ec2a864
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09040691B2

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