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Pyridine → 4-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)benzonitrile

HRID 2218893
ノート
印刷プレビュー

反応式

HRID 2218893 の反応式
[C:1]([CH:5]1[CH2:10][CH2:9][CH:8]([C:11]2[CH:19]=[CH:18][C:14]([CH:15]=[N:16]O)=[CH:13][C:12]=2[N:20]2[CH2:25][CH2:24][N:23]([CH2:26][CH2:27][CH2:28][CH3:29])[CH2:22][CH2:21]2)[CH2:7][CH2:6]1)([CH3:4])([CH3:3])[CH3:2].C1(S(Cl)(=O)=O)C=CC=CC=1.N1C=CC=CC=1>O1CCCC1>[C:1]([CH:5]1[CH2:6][CH2:7][CH:8]([C:11]2[CH:19]=[CH:18][C:14]([C:15]#[N:16])=[CH:13][C:12]=2[N:20]2[CH2:25][CH2:24][N:23]([CH2:26][CH2:27][CH2:28][CH3:29])[CH2:22][CH2:21]2)[CH2:9][CH2:10]1)([CH3:4])([CH3:3])[CH3:2]
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 1049PyridineHCID 7369Benzenesulfonyl chlorideHCID 740205524-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)benzaldehydeoxime

生成物 1

HCID 114064144-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)benzonitrile収率 74.7%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A mixture of the crude product of 4-(4-t-butylcyclohexyl)-3-(4-butylpiperazine-1-yl)benzaldehydeoxime produced in Example (101c) (269 mg), benzenesulfonyl chloride (0.11 mL, 0.862 mmol), pyridine (0.11 ml, 1.36 mmol) and tetrahydrofuran (15 mL) was refluxed for 4 hours and 30 minutes. After then distilling off tetrahydrofuran partially in the reaction mixture under reduced pressure, chloroform was added and the mixture was further refluxed for 1 hour. The reaction mixture was concentrated under reduced pressure, the obtained residue was poured into ice water, and then ethyl acetate and saturated aqueous solution of ammonium chloride were added and extraction was performed with ethyl acetate. The separated organic layer was washed twice with saturated aqueous ammonium chloride and once with brine, and then dried over anhydrous sodium sulfate. The desiccant was filtered off, and the filtrate was concentrated under reduced pressure to give a residue, which was purified by NH silica gel column chromatography (ethyl acetate/hexane, followed by ethyl acetate/methanol), to give 192 mg of the title compound as an ochre oil.

後処理

  1. temperaturewas refluxed for 4 hours and 30 minutes
  2. distillationAfter then distilling off tetrahydrofuran partially in the reaction mixture under reduced pressure, chloroform
  3. additionwas added
  4. temperaturethe mixture was further refluxed for 1 hour
  5. concentrationThe reaction mixture was concentrated under reduced pressure
  6. additionthe obtained residue was poured into ice water
  7. additionethyl acetate and saturated aqueous solution of ammonium chloride were added
  8. extractionextraction
  9. washThe separated organic layer was washed twice with saturated aqueous ammonium chloride and once with brine
  10. dry with materialdried over anhydrous sodium sulfate
  11. filtrationThe desiccant was filtered off
  12. concentrationthe filtrate was concentrated under reduced pressure
  13. customto give a residue, which
  14. customwas purified by NH silica gel column chromatography (ethyl acetate/hexane, followed by ethyl acetate/methanol)

出典と根拠

ORDレコード
ord-988460fd99a54169b0533df4535b7e80
出典データセット
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07410971B2

反応ノート

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