2-Naphthalenecarboxaldehyde → N-[6{(Naphthalen-2-ylmethyl)-amino}-hexyl]-2-nitrobenzenesulfonamide

HRID 322480ノート

反応式

HRID 322480 の反応式
Cl.[NH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][NH:9][S:10]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[N+:19]([O-:21])=[O:20])(=[O:12])=[O:11].[CH:22]1[C:31]2[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=2)[CH:25]=[CH:24][C:23]=1[CH:32]=O>C1(C)C=CC=CC=1>[CH:22]1[C:31]2[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=2)[CH:25]=[CH:24][C:23]=1[CH2:32][NH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][NH:9][S:10]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[N+:19]([O-:21])=[O:20])(=[O:11])=[O:12]

参加物

4

実験手順

A mixture of N-(6-Aminohexyl)-2-nitrobenzenesulfonamide hydrochloride (0.67 g, 2.0 mmol) and 2-naphthaldehyde (0.32 g, 2.1 mmol) in 75 mL of toluene was refluxed using a Dean Stark trap for 20 h. The reaction mixture was concentrated in vacuo. The residue was dissolved in ethanol (40 mL) and sodium borohyride (0.020 g, 6.0 mmol) was added. After the reaction was complete (6 h), the solvent was evaporated and residue taken up in 30 mL of saturated sodium chloride solution and extracted with ethyl acetate (3×40 mL), washed with saturated sodium chloride solution, dried over sodium sulfate and concentrated to afford an oil. The oil was flash chromatographed over silica gel to afford the titled compound (0.16 g, 37%) which was converted into hydrochloride salt (mp 169° C.).

後処理

  1. temperaturewas refluxed
  2. customfor 20 h
  3. concentrationThe reaction mixture was concentrated in vacuo
  4. dissolutionThe residue was dissolved in ethanol (40 mL)
  5. additionsodium borohyride (0.020 g, 6.0 mmol) was added
  6. custom(6 h)
  7. customthe solvent was evaporated
  8. extractionextracted with ethyl acetate (3×40 mL)
  9. washwashed with saturated sodium chloride solution
  10. dry with materialdried over sodium sulfate
  11. concentrationconcentrated
  12. customto afford an oil
  13. customchromatographed over silica gel

出典と根拠

ORDレコード
ord-c7001f52dbcb45c29b63eeee31190511
出典データセット
uspto-grants-2001_04
特許番号
US06211241B1

反応ノート

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