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Sulfuric Acid → 3-Chloroimidazo[1,2-a]pyridin-8-amine

HRID 1955004
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HRID 1955004 반응식
[Cl:1][C:2]1[N:6]2[CH:7]=[CH:8][CH:9]=[C:10]([NH:11]C(=O)C(C)(C)C)[C:5]2=[N:4][C:3]=1C.S(=O)(=O)(O)O.[OH-].[Na+]>O>[NH2:11][C:10]1[C:5]2[N:6]([C:2]([Cl:1])=[CH:3][N:4]=2)[CH:7]=[CH:8][CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 232941713-Chloro-2-methyl-8-pivaloylaminoimidazo[1,2-a]pyridine

생성물 1

HCID 232941763-Chloroimidazo[1,2-a]pyridin-8-amine

시약·촉매·용매 1

HCID 962Water용매

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온도
100 °C

실험 절차

A suspension of 3-chloro-2-methyl-8-pivaloylaminoimidazo[1,2-a]pyridine (4.0 g, 15 mmol) in 60% strength sulfuric acid (25 ml) is stirred at 100° C. for 1 h. After cooling to RT, water (100 ml) is added and the mixture is adjusted to pH 10 using 10 N sodium hydroxide solution. It is then extracted with ethyl acetate (3×50 ml). The combined organic extracts are washed with water (50 ml), dried over magnesium sulfate and concentrated. The residue is taken up in boiling toluene, clarified with silica gel and crystallized. The title compound is isolated as a beige solid. Yield 1.9 g (70%), m.p. 126-127° C.

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후처리

  1. temperatureAfter cooling to RT
  2. extractionIt is then extracted with ethyl acetate (3×50 ml)
  3. washThe combined organic extracts are washed with water (50 ml)
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated
  6. customcrystallized

출처 및 근거

ORD 기록
ord-c316d10b31fa49a89102054287afad6f
출처 데이터셋
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06124313

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