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N-bromobutanimide → 3-Bromo-8-phenylimidazo[1,2-a]pyridine

HRID 1982538
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반응식

HRID 1982538 반응식
[C:1]1([C:7]2[C:8]3[N:9]([CH:13]=[CH:14][N:15]=3)[CH:10]=[CH:11][CH:12]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:16]N1C(=O)CCC1=O>C(Cl)Cl>[Br:16][C:13]1[N:9]2[CH:10]=[CH:11][CH:12]=[C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[C:8]2=[N:15][CH:14]=1
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참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 137640278-Phenylimidazo[1,2-a]pyridine

생성물 1

HCID 233169583-Bromo-8-phenylimidazo[1,2-a]pyridine

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Combine 2 g (10.3 mmol) of the product from Example 4 with 1.8 g (10.3 mmol) of N-bromosuccinimide in 50 ml of methylene chloride, and stir for 10 minutes at room temperature. Wash the reaction mixture with 50 ml of 10% potassium carbonate. Dry the methylene chloride layer over sodium sulfate, treat with charcoal, filter, and remove the solvent in vacuo. Crystallize the residue from ether to provide the title compound.

후처리

  1. washWash the reaction mixture with 50 ml of 10% potassium carbonate
  2. dry with materialDry the methylene chloride layer over sodium sulfate
  3. additiontreat with charcoal
  4. filtrationfilter
  5. customremove the solvent in vacuo
  6. customCrystallize the residue from ether

출처 및 근거

ORD 기록
ord-72484a54a434498d87ac3b9620ad69f4
출처 데이터셋
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04596872

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