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Water → 7-(methylthio)-2-(4-nitrophenyl)-2H-pyrazolo[4,3-d]pyrimidine

HRID 1786958
ノート
印刷プレビュー

反応式

HRID 1786958 の反応式
[CH3:1][S:2][C:3]1[C:4]2[NH:11][N:10]=[CH:9][C:5]=2[N:6]=[CH:7][N:8]=1.CC(C)([O-])C.[K+].F[C:19]1[CH:24]=[CH:23][C:22]([N+:25]([O-:27])=[O:26])=[CH:21][CH:20]=1.O>CN(C)C=O>[CH3:1][S:2][C:3]1[C:4]2[C:5](=[CH:9][N:10]([C:19]3[CH:24]=[CH:23][C:22]([N+:25]([O-:27])=[O:26])=[CH:21][CH:20]=3)[N:11]=2)[N:6]=[CH:7][N:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 9590p-FluoronitrobenzeneHCID 23665647Potassium tert-butoxideHCID 552958947-(methylthio)-1H-pyrazolo[4,3-d]pyrimidine

生成物 1

HCID 675207817-(methylthio)-2-(4-nitrophenyl)-2H-pyrazolo[4,3-d]pyrimidine収率 99.5%

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

実験手順

To a solution of 7-(methylthio)-1H-pyrazolo[4,3-d]pyrimidine (500 mg) in N,N-dimethylformamide (10 mL) was added potassium tert-butoxide (405 mg) under ice-cooling, and the mixture was stirred at room temperature for 10 min. Subsequently, 1-fluoro-4-nitrobenzene (465 mg) was added, and the mixture was stirred at 70° C. for 30 min. After the completion of the reaction, water was added to the reaction mixture and the mixture was stirred at room temperature for 30 min. The resultant solid was collected by filtration, washed with diisopropyl ether and dried to give the title compound (860 mg) as brown crystals.

後処理

  1. temperaturecooling
  2. stirringthe mixture was stirred at 70° C. for 30 min
  3. additionwas added to the reaction mixture
  4. stirringthe mixture was stirred at room temperature for 30 min
  5. filtrationThe resultant solid was collected by filtration
  6. washwashed with diisopropyl ether
  7. customdried

出典と根拠

ORDレコード
ord-3695b16b65e44800aa8c0af10d9082ed
出典データセット
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07507740B2

反応ノート

読み込み中…

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