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N-(6-Chloro-4-o-tolyl-pyridin-3-yl)-N-methyl-3,5-bis-trifluoromethyl-benzamide → N-(6-Ethyl-4-o-tolyl-pyridin-3-yl)-N-methyl-3,5-bis-trifluoromethyl-benzamide

HRID 878254
ノート
印刷プレビュー

反応式

HRID 878254 の反応式
Cl[C:2]1[N:7]=[CH:6][C:5]([N:8]([CH3:25])[C:9](=[O:24])[C:10]2[CH:15]=[C:14]([C:16]([F:19])([F:18])[F:17])[CH:13]=[C:12]([C:20]([F:23])([F:22])[F:21])[CH:11]=2)=[C:4]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=2[CH3:32])[CH:3]=1.[CH2:33]([Zn]CC)[CH3:34]>C1COCC1>[CH2:33]([C:2]1[N:7]=[CH:6][C:5]([N:8]([CH3:25])[C:9](=[O:24])[C:10]2[CH:11]=[C:12]([C:20]([F:23])([F:22])[F:21])[CH:13]=[C:14]([C:16]([F:19])([F:18])[F:17])[CH:15]=2)=[C:4]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=2[CH3:32])[CH:3]=1)[CH3:34]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 60197100N-(6-Chloro-4-o-tolyl-pyridin-3-yl)-N-methyl-3,5-bis-trifluoromethyl-benzamideHCID 178418750HCID 178418750、化合物

生成物 1

HCID 86670805N-(6-Ethyl-4-o-tolyl-pyridin-3-yl)-N-methyl-3,5-bis-trifluoromethyl-benzamide

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of N-(6-chloro-4-o-tolylpyridin-3-yl)-N-methyl-3,5-bis(trifluoromethyl)-benzamide (0.1 g, 212 μmol, example 12) in THF (1 mL) were added tetrakis(triphenyl-phosphine)palladium(0) (12.2 mg, 10.6 μmol) and diethylzinc (1M solution in n-hexane, 137 μL, 137 μmol) and the brown solution was stirred at reflux for 16 hours. The solvent was evaporated and the brown gum was diluted with 1M aqueous HCl and EtOAc and the layers were separated. The aqueous layer was extracted twice with EtOAc. The organic layers were washed with brine, dried over MgSO4, filtered, treated with silica gel and evaporated. The compound was purified by silica gel chromatography on a 10 g column using an MPLC system eluting with a gradient of n-heptane:EtOAc (100:0 to 30:70). Light yellow solid (0.051 g; 51%). MS (ESI): m/z=467.16 [M+H]+.

後処理

  1. temperatureat reflux for 16 hours
  2. customThe solvent was evaporated
  3. additionthe brown gum was diluted with 1M aqueous HCl and EtOAc
  4. customthe layers were separated
  5. extractionThe aqueous layer was extracted twice with EtOAc
  6. washThe organic layers were washed with brine
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. additiontreated with silica gel
  10. customevaporated
  11. customThe compound was purified by silica gel chromatography on a 10 g column
  12. washeluting with a gradient of n-heptane:EtOAc (100:0 to 30:70)

出典と根拠

ORDレコード
ord-14e6fd6ddb774ef89569f89b6b9505e0
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08987307B2

反応ノート

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