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Hydrochloric Acid → HCID 18538785、化合物

HRID 412917
ノート
印刷プレビュー

反応式

HRID 412917 の反応式
[CH2:1]([NH2:4])[CH2:2][CH3:3].C(N(CC)CC)C.[C:12]([N:15]1[CH2:20][CH2:19][CH:18]([CH2:21][C:22]2[CH:27]=[CH:26][C:25]([S:28](Cl)(=[O:30])=[O:29])=[CH:24][CH:23]=2)[CH2:17][CH2:16]1)(=[O:14])[CH3:13].Cl>C1COCC1>[C:12]([N:15]1[CH2:20][CH2:19][CH:18]([CH2:21][C:22]2[CH:27]=[CH:26][C:25]([S:28]([NH:4][CH2:1][CH2:2][CH3:3])(=[O:30])=[O:29])=[CH:24][CH:23]=2)[CH2:17][CH2:16]1)(=[O:14])[CH3:13]
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 313Hydrochloric AcidHCID 7852PropylamineHCID 8471TriethylamineHCID 226766334-[(1-Acetylpiperidin-4-yl)methyl]benzene-1-sulfonyl chloride

生成物 1

HCID 18538785HCID 18538785、化合物収率 71.5%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

1-Propylamine (0.586 ml, 7.13 mmol) and triethylamine (0.993 ml, 7.13 mmol) were added to a solution of 4-(1-acetylpiperidin-4-ylmethyl)benzenesulfonylchloride (1.5 g, 4.75 mmol) in THF (20 ml) and this mixture was refluxed for 5 h. After having been cooled, 1N hydrochloric acid (20 ml) was added. The resulting mixture was extracted with ethyl acetate (20 ml×2). The combined organic layers were washed with saturated sodium chloride solution (40 ml), and then dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by flash column chromatography (silica gel 25 g, ethyl acetate to ethyl acetate/methanol=10/1) to give the title compound (1.15 g, 71%) as pale yellow oil.

後処理

  1. temperaturethis mixture was refluxed for 5 h
  2. temperatureAfter having been cooled
  3. extractionThe resulting mixture was extracted with ethyl acetate (20 ml×2)
  4. washThe combined organic layers were washed with saturated sodium chloride solution (40 ml)
  5. dry with materialdried over anhydrous sodium sulfate
  6. customThe solvent was removed under reduced pressure
  7. customthe residue was purified by flash column chromatography (silica gel 25 g, ethyl acetate to ethyl acetate/methanol=10/1)

出典と根拠

ORDレコード
ord-a5ecea6742994ff781885a5cb06a1c0e
出典データセット
uspto-grants-2003_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06562978B1

反応ノート

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