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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Peroxide → HCID 178433625, 화합물

HRID 973477
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HRID 973477 반응식
[CH3:1][C:2]1[NH:3][C:4]2[CH:9]=[CH:8][N:7]=[CH:6][C:5]=2[N:10]=1.[OH:11]O>C(O)(=O)C>[CH3:1][C:2]1[NH:10][C:5]2[CH:6]=[N:7][CH:8]=[CH:9][C:4]=2[N+:3]=1[O-:11]
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참가 물질

4

반응물 2

HCID 784Hydrogen PeroxideHCID 178432317HCID 178432317, 화합물

생성물 1

HCID 178433625HCID 178433625, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

Following the method of Chem. Pharm. Bull., 12, 866 (1964), a solution of 2-methylimidazo[4,5-c]pyridine (5.65 g, 42.5 mmol) in 30% aqueous hydrogen peroxide (15 ml) and glacial acetic acid was stirred at 60° C. for 6 days. The volatiles were removed under reduced pressure and the residue was dissolved in ethanol and treated with solid anhydrous potassium carbonate. The solid was filtered off, washed with ethanol, and the filtrate was concentrated under reduced pressure. The crude product was purified by flash chromatography eluting with 10-30% water in acetone. Fractions containing the product were concentrated under reduced pressure, redissolved in isopropanol/toluene, 1:1 (200 ml) and re-evaporated to give the title compound, as a hygroscopic solid, (2.94 g, 46%).

후처리

  1. customThe volatiles were removed under reduced pressure
  2. dissolutionthe residue was dissolved in ethanol
  3. additiontreated with solid anhydrous potassium carbonate
  4. filtrationThe solid was filtered off
  5. washwashed with ethanol
  6. concentrationthe filtrate was concentrated under reduced pressure
  7. customThe crude product was purified by flash chromatography
  8. washeluting with 10-30% water in acetone
  9. additionFractions containing the product
  10. concentrationwere concentrated under reduced pressure
  11. dissolutionredissolved in isopropanol/toluene
  12. custom1:1 (200 ml) and re-evaporated

출처 및 근거

ORD 기록
ord-d097f73b73d54829a7304c7919e95452
출처 데이터셋
uspto-grants-1991_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05063237

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