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Bromine → HCID 86644690、化合物

HRID 1097476
ノート
印刷プレビュー

反応式

HRID 1097476 の反応式
[NH2:1][C:2]1[CH:23]=[CH:22][C:5]([O:6][C:7]2[C:8]([Cl:21])=[CH:9][C:10]([F:20])=[C:11]([NH:13][C:14](=[O:19])[C:15]([F:18])([F:17])[F:16])[CH:12]=2)=[C:4]([C:24]#[N:25])[CH:3]=1.[S-:26][C:27]#[N:28].[K+].BrBr>C(O)(=O)C>[NH2:28][C:27]1[S:26][C:3]2[C:4]([C:24]#[N:25])=[C:5]([O:6][C:7]3[C:8]([Cl:21])=[CH:9][C:10]([F:20])=[C:11]([NH:13][C:14](=[O:19])[C:15]([F:16])([F:17])[F:18])[CH:12]=3)[CH:22]=[CH:23][C:2]=2[N:1]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 24408BromineHCID 516872Potassium thiocyanateHCID 86644689HCID 86644689、化合物

生成物 1

HCID 86644690HCID 86644690、化合物収率 61.5%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

実験手順

To a solution of N-[5-(4-amino-2-cyanophenoxy)-4-chloro-2-fluorophenyl]-2,2,2-trifluoroacetamide (1.0 g, 2.68 mmol) in acetic acid (20 mL) was added potassium thiocyanate (1.3 g, 13.4 mmol), and the mixture was stirred at room temperature for 10 min. A solution of bromine (513 mg, 3.21 mmol) in acetic acid (10 mL) was slowly added dropwise to the obtained solution. After the completion of the dropwise addition, the mixture was stirred at room temperature for 12 hr. The resulting yellow insoluble material was filtered off and washed with acetic acid. The filtrate and washings were combined and the mixture was concentrated under reduced pressure. The obtained residue was suspended in ethyl acetate (150 mL), washed successively with 5% aqueous sodium hydrogen carbonate solution (150 mL×2) and saturated brine (150 mL), and dried over anhydrous sodium sulfate. Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=30/70→80/20), and the obtained solution was concentrated under reduced pressure. The residue was recrystallized from ethyl acetate/n-hexane to give the title compound (0.71 g, 60%) as a white powder.

後処理

  1. additionAfter the completion of the dropwise addition
  2. stirringthe mixture was stirred at room temperature for 12 hr
  3. filtrationThe resulting yellow insoluble material was filtered off
  4. washwashed with acetic acid
  5. concentrationthe mixture was concentrated under reduced pressure
  6. washwashed successively with 5% aqueous sodium hydrogen carbonate solution (150 mL×2) and saturated brine (150 mL)
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationInsoluble material was filtered off
  9. concentrationthe filtrate was concentrated under reduced pressure
  10. customThe obtained residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=30/70→80/20)
  11. concentrationthe obtained solution was concentrated under reduced pressure
  12. customThe residue was recrystallized from ethyl acetate/n-hexane

出典と根拠

ORDレコード
ord-6c9503eb4a06430f9d66c5ead211d227
出典データセット
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08143258B2

反応ノート

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