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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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[6-(1H-Imidazol-1-yl)pyridin-3-yl]methanol → 6-(1H-iMidazol-1-yl)nicotinaldehyde

HRID 1252486
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HRID 1252486 반응식
[N:1]1([C:6]2[CH:11]=[CH:10][C:9]([CH2:12][OH:13])=[CH:8][N:7]=2)[CH:5]=[CH:4][N:3]=[CH:2]1>C(Cl)(Cl)Cl.O=[Mn]=O>[N:1]1([C:6]2[CH:11]=[CH:10][C:9]([CH:12]=[O:13])=[CH:8][N:7]=2)[CH:5]=[CH:4][N:3]=[CH:2]1
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참가 물질

4

반응물 1

HCID 14207630[6-(1H-Imidazol-1-yl)pyridin-3-yl]methanol

생성물 1

HCID 140316506-(1H-iMidazol-1-yl)nicotinaldehyde

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 6212Chloroform용매

실험 절차

MnO2 (18.17 g) is added to a solution of the hydroxy methyl compound of Step 3. above (6.1 g) in CHCl3, and the resulting reaction mixture heated to reflux for 22 hours, allowed to cool, filtered, and the organic layer evaporated affording the desired product as a white solid. M.P.=136°-137.5° C.

후처리

  1. temperatureheated
  2. temperatureto reflux for 22 hours
  3. temperatureto cool
  4. filtrationfiltered
  5. customthe organic layer evaporated

출처 및 근거

ORD 기록
ord-195183cb84d44d358334162d164b4776
출처 데이터셋
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04743608

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