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Iodine → 2-Amino-5-chloro-3-iodopyridine

HRID 58651
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HRID 58651 반응식
[I:1]I.[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([NH2:10])=[N:8][CH:9]=1>C(O)C.S([O-])([O-])(=O)=O.[Ag+2]>[Cl:3][C:4]1[CH:5]=[C:6]([I:1])[C:7]([NH2:10])=[N:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 807IodineHCID 661742-Amino-5-chloropyridine

생성물 1

HCID 110760102-Amino-5-chloro-3-iodopyridine수율 64%

시약·촉매·용매 2

HCID 178418844HCID 178418844, 화합물촉매HCID 702Ethanol용매

실험 절차

Iodine (7.55 g; 29.73 mmol) was added to a mixture of 5-chloropyridin-2-amine (3.00 g; 22.87 mmol) and silver sulphate (9.36 g; 29.73 mmol) in ethanol (150 mL) and the mixture was stirred overnight at room temperature. The mixture was filtered over celite, washed with ethanol, and the filtrate concentrated under reduced pressure. The residue was dissolved in dichloromethane, and the solution was washed with a saturated aqueous solution of sodium thiosulphate. The organic layer was dried over magnesium sulphate, concentrated under reduced pressure and the crude material purified by flash chromatography on silica gel (eluent: 0 to 30% of ethyl acetate in heptane) to give 3.71 g (64%) of 5-chloro-3-iodopyridin-2-amine as a beige solid.

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후처리

  1. filtrationThe mixture was filtered over celite
  2. washwashed with ethanol
  3. concentrationthe filtrate concentrated under reduced pressure
  4. dissolutionThe residue was dissolved in dichloromethane
  5. washthe solution was washed with a saturated aqueous solution of sodium thiosulphate
  6. dry with materialThe organic layer was dried over magnesium sulphate
  7. concentrationconcentrated under reduced pressure
  8. customthe crude material purified by flash chromatography on silica gel (eluent: 0 to 30% of ethyl acetate in heptane)

출처 및 근거

ORD 기록
ord-601e897bc3144f69904f9d03319b7ee7
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434722B2

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