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Water → 3-Iodopyridine-2,6-diamine

HRID 77832
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HRID 77832 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([NH2:8])[N:3]=1.[I:9]N1C(=O)CCC1=O.O>CS(C)=O>[I:9][C:7]1[C:2]([NH2:1])=[N:3][C:4]([NH2:8])=[CH:5][CH:6]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 88612,6-DiaminopyridineHCID 120273N-Iodosuccinimide

생성물 1

HCID 4762183-Iodopyridine-2,6-diamine수율 22.8%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

2,6-Diaminopyridine (100 g, 916 mmol) was dissolved in dimethyl sulfoxide (400 mL), and N-iodosuccinimide (100 g, 445 mmol) was added in one portion while stirring at room temperature. The reaction solution was stirring for 10 minutes at room temperature. Water (3.5 L) was added to the reaction solution, and the precipitated solids were filtered out. The resulting aqueous layer was extracted with ethyl acetate (1.3 L) 3 times. The ethyl acetate layers were combined and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel chromatography (heptane:ethyl acetate=2:3) to obtain the title compound (23.8 g, 22.8%).

후처리

  1. stirringThe reaction solution was stirring for 10 minutes at room temperature
  2. filtrationthe precipitated solids were filtered out
  3. extractionThe resulting aqueous layer was extracted with ethyl acetate (1.3 L) 3 times
  4. customthe solvent was evaporated under a reduced pressure
  5. customThe residue was purified by silica gel chromatography (heptane:ethyl acetate=2:3)

출처 및 근거

ORD 기록
ord-3aa85e0c537f40388de71e7309cd7eb1
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08841327B2

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