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HCID 68469062, 화합물 → HCID 68470026, 화합물

HRID 503019
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HRID 503019 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:9]([CH3:24])[C:10]([C:13]([CH3:23])([CH3:22])[CH:14]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[OH:15])=[N:11][N:12]=1>[O-2].[O-2].[Mn+4].C(Cl)Cl>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:9]([CH3:24])[C:10]([C:13]([CH3:22])([CH3:23])[C:14]([C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=2)=[O:15])=[N:11][N:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 68469062HCID 68469062, 화합물

생성물 1

HCID 68470026HCID 68470026, 화합물수율 73.7%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매2회HCID 6344Dichloromethane용매

실험 절차

Manganese dioxide (955 mg) was gradually added to a methylene chloride (4.8 ml) solution of 2-[5-(2-chlorophenyl)-4-methyl-4H-1,2,4-triazol-3-yl]-2-methyl-1-phenylpropan-1-ol (191 mg) under ice cooling. The reaction mixture was stirred at room temperature for 3 hours and then manganese dioxide (955 mg) was added thereto, followed by stirring at room temperature for another 18.5 hours. Then, the mixture was subjected to filtration through celite. The filtrate was subjected to evaporation under reduced pressure and then purified by silica gel column chromatography (chloroform:methanol=50:1) to obtain 2-[5-(2-chlorophenyl)-4-methyl-4H-1,2,4-triazol-3-yl]-2-methyl-1-phenylpropan-1-one (140 mg).

후처리

  1. stirringby stirring at room temperature for another 18.5 hours
  2. filtrationThen, the mixture was subjected to filtration through celite
  3. customThe filtrate was subjected to evaporation under reduced pressure
  4. custompurified by silica gel column chromatography (chloroform:methanol=50:1)

출처 및 근거

ORD 기록
ord-7815ff8468a0479888974c67024bef5b
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07776897B2

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