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(2-{[2-(Dimethylamino)ethyl]amino}-4,6-dimethylpyridin-3-yl)methanol → HCID 20477991, 화합물

HRID 904899
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인쇄 미리보기

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HRID 904899 반응식
[CH3:1][N:2]([CH3:16])[CH2:3][CH2:4][NH:5][C:6]1[C:11]([CH2:12][OH:13])=[C:10]([CH3:14])[CH:9]=[C:8]([CH3:15])[N:7]=1>C(Cl)Cl.[O-2].[O-2].[Mn+4]>[CH3:1][N:2]([CH3:16])[CH2:3][CH2:4][NH:5][C:6]1[N:7]=[C:8]([CH3:15])[CH:9]=[C:10]([CH3:14])[C:11]=1[CH:12]=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 20477995(2-{[2-(Dimethylamino)ethyl]amino}-4,6-dimethylpyridin-3-yl)methanol

생성물 1

HCID 20477991HCID 20477991, 화합물

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 6344Dichloromethane용매

실험 절차

A solution of crude 2-(2-dimethylaminoethylamino)-3-hydroxymethyl-4,6-dimethylpyridine (15.0 g, 67 mmol) in methylene chloride (300 ml) containing a suspension of activated manganese dioxide (35 g) is refluxed for 5 hours. The solution is filtered hot and the manganese dioxide re-extracted with hot methylene chloride. The combined extracts are filtered through charcoal and evaporated to give 12.0 g of crude title D product.

후처리

  1. temperatureis refluxed for 5 hours
  2. filtrationThe solution is filtered hot
  3. extractionthe manganese dioxide re-extracted with hot methylene chloride
  4. filtrationThe combined extracts are filtered through charcoal
  5. customevaporated
  6. customto give 12.0 g of crude title D product

출처 및 근거

ORD 기록
ord-459c9d1443384610b59d84eaa51a49ad
출처 데이터셋
uspto-grants-1983_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04420615

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