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Chlorosuccinimide → 4-Bromo-5-chloropyridin-2-amine

HRID 1521940
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HRID 1521940 반응식
[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([NH2:8])[CH:3]=1.[Cl:9]N1C(=O)CCC1=O>CN(C)C=O>[Br:1][C:2]1[C:7]([Cl:9])=[CH:6][N:5]=[C:4]([NH2:8])[CH:3]=1
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참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 6932822-Amino-4-bromopyridine

생성물 1

HCID 534854184-Bromo-5-chloropyridin-2-amine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 4-bromopyridin-2-amine (500 mg, 2.89 mmol) in N,N-dimethylformamide (5 mL) was added N-chlorosuccinimide (463 mg, 3.47 mmol) and the mixture was stirred at room temperature for 12 hours. The mixture was filtered through diatomaceous earth and concentrated and the residue was dissolved in ethyl acetate. The solution was washed with water and brine, dried over anhydrous sodium sulfate, filtered, and concentrated to afford the crude title compound. Purification by column chromatography (silica gel, 30% ethyl acetate in hexane) afforded the title compound.

후처리

  1. filtrationThe mixture was filtered through diatomaceous earth
  2. concentrationconcentrated
  3. dissolutionthe residue was dissolved in ethyl acetate
  4. washThe solution was washed with water and brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto afford the crude title compound
  9. customPurification by column chromatography (silica gel, 30% ethyl acetate in hexane)

출처 및 근거

ORD 기록
ord-d14e4019191643db9bdf739666e4969a
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073922B2

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