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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Thionyl Chloride → 2,4-Dimethylpyridin-3-amine

HRID 383703
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HRID 383703 반응식
[CH3:1][C:2]1[N:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:3]=1C(O)=O.S(Cl)(Cl)=O.[N-:16]=[N+]=[N-].[Na+]>O>[CH3:1][C:2]1[C:3]([NH2:16])=[C:7]([CH3:11])[CH:8]=[CH:9][N:10]=1
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참가 물질

5

반응물 3

HCID 24386Thionyl ChlorideHCID 33557Sodium AzideHCID 15125612,4-Dimethyl-3-pyridinecarboxylic acid

생성물 1

HCID 149107812,4-Dimethylpyridin-3-amine수율 74%

시약·촉매·용매 1

HCID 962Water용매

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온도
60 °C

실험 절차

A mixture of 1a (0.98 g, 6.5 mmol) and thionyl chloride (5 ml) was heated to 60° C. for 1 hour. The mixture was concentrated to dryness. The mixture was then dissolved in acetone (10 ml) prior to the addition of NaN3 (0.65 g, 10 mmol) and water (5 ml). The solution was heated to 70° C. for 1 hour. Acetone was evaporated from the reaction mixture which was washed with brine and extracted with ethyl acetate. The organic layer was dried over MgSO4, concentrated and chromatographed to yield 1b (0.585 g, 4.79 mmol, 74%).

후처리

  1. concentrationThe mixture was concentrated to dryness
  2. dissolutionThe mixture was then dissolved in acetone (10 ml)
  3. temperatureThe solution was heated to 70° C. for 1 hour
  4. customAcetone was evaporated from the reaction mixture which
  5. washwas washed with brine
  6. extractionextracted with ethyl acetate
  7. dry with materialThe organic layer was dried over MgSO4
  8. concentrationconcentrated
  9. customchromatographed

출처 및 근거

ORD 기록
ord-161e9a64b288476da7e8ad850f7924be
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367684B2

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