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Sulfuryl chloride → 1H-Pyrrolo[2,3-b]pyridine-3-acetonitrile, 2-chloro-

HRID 1756101
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HRID 1756101 반응식
[C:1]([CH2:3][C:4]1[C:12]2[C:7](=[N:8][CH:9]=[CH:10][CH:11]=2)[NH:6][CH:5]=1)#[N:2].S(Cl)([Cl:16])(=O)=O>C(O)(=O)C>[Cl:16][C:5]1[NH:6][C:7]2=[N:8][CH:9]=[CH:10][CH:11]=[C:12]2[C:4]=1[CH2:3][C:1]#[N:2]
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참가 물질

4

반응물 2

HCID 24648Sulfuryl chlorideHCID 21911990(1H-Pyrrolo[2,3-b]pyridin-3-yl)acetonitrile

생성물 1

HCID 193925831H-Pyrrolo[2,3-b]pyridine-3-acetonitrile, 2-chloro-

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

3-cyanomethylpyrrolo[2,3-b]pyridine (1,55 g, 0.098 mol) was treated in 5 ml acetic acid with an equimolecular amount of sulfurylchloride at 0° C. for 5 min. The mixture was allowed to warm to room temperature and was stirred 5 min. After evaporation the residue was dissolved in methylen chloride and was treated with bicarbonate. The organic layer was separated, dried over Na2SO4 and the solvent was removed under reduced pressure. Chromatography on silica gel eluting with ethyl acetate gave the desired product. (0,4 g 21%).

후처리

  1. customAfter evaporation the residue
  2. dissolutionwas dissolved in methylen chloride
  3. additionwas treated with bicarbonate
  4. customThe organic layer was separated
  5. dry with materialdried over Na2SO4
  6. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-35ec616ca9f1410dbe3bae3a04a93e87
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05439917

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