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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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8-(4-Nitrophenyl)imidazo[1,2-a]pyridine → Benzenamine,4-imidazo[1,2-a]pyridin-8-yl-

HRID 1982540
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HRID 1982540 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[C:11]3[N:12]([CH:16]=[CH:17][N:18]=3)[CH:13]=[CH:14][CH:15]=2)=[CH:6][CH:5]=1)([O-])=O>C(O)(=O)C.[Fe]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([C:10]2[C:11]3[N:12]([CH:16]=[CH:17][N:18]=3)[CH:13]=[CH:14][CH:15]=2)=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 233169598-(4-Nitrophenyl)imidazo[1,2-a]pyridine

생성물 1

HCID 13810555Benzenamine,4-imidazo[1,2-a]pyridin-8-yl-

시약·촉매·용매 2

HCID 23925Iron촉매HCID 176Acetic Acid용매

실험 절차

Add 45 g of iron powder to a solution of 15 g (62.7 mmol) of the product from Example 19 in 400 ml of 75% acetic acid. Heat to 60°-70° C. for 2 hr. Filter the reaction mixture over celite and concentrate the filtrate to approximately 50 ml under vacuum. Neutralize the residue with saturated sodium carbonate solution and extract with three 200 ml portions of methylene chloride. Dry the combined extracts over sodium sulfate, treat with charcoal and remove the solvent in vacuo. Crystallize the residue from ether to provide the title compound.

후처리

  1. temperatureHeat to 60°-70° C. for 2 hr
  2. filtrationFilter the reaction mixture over celite and
  3. concentrationconcentrate the filtrate to approximately 50 ml under vacuum
  4. extractionNeutralize the residue with saturated sodium carbonate solution and extract with three 200 ml portions of methylene chloride
  5. dry with materialDry the combined extracts over sodium sulfate
  6. additiontreat with charcoal
  7. customremove the solvent in vacuo
  8. customCrystallize the residue from ether

출처 및 근거

ORD 기록
ord-9129e40b0db1457f91d0a0dff5c0082a
출처 데이터셋
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04596872

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