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Sodium hydride → 5-(6,7,8,9-Tetrahydro-5H-pyrido[2,3-b]azepin-2-yl)-pentanoic acid methylamide

HRID 2187386
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反応式

HRID 2187386 の反応式
[CH3:1][NH:2][C:3](=[O:19])[CH2:4][CH2:5][CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH2:16][CH2:17][NH2:18])=[CH:10][N:9]=1.[H-].[Na+]>>[CH3:1][NH:2][C:3](=[O:19])[CH2:4][CH2:5][CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]2[CH2:14][CH2:15][CH2:16][CH2:17][NH:18][C:10]=2[N:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 24758Sodium hydrideHCID 220826725-[5-(4-Aminobutyl)pyridin-2-YL]-N-methylpentanamide

生成物 1

HCID 220826735-(6,7,8,9-Tetrahydro-5H-pyrido[2,3-b]azepin-2-yl)-pentanoic acid methylamide

実験手順

A mixture of 11-7 (24 g, 91.2 mmol) and NaH (10.9 g of a 60% weight dispersion in mineral oil, 273 mmol) in xylenes (500 mL) was purged with argon for 30 min, and then heated at reflux for 72 hours. The mixture was cooled, quenched with ethanol, diluted with 10% aqueous potassium carbonate and extracted with ethyl acetate. The organics were dried over MgSO4, and concentrated to an oil. The residue was chromatographed on silica gel (70:25:5 CHCl3/EtOAc/MeOH/H2O) to give 11-8 as a white solid.

後処理

  1. customwas purged with argon for 30 min
  2. temperatureheated
  3. temperatureat reflux for 72 hours
  • temperatureThe mixture was cooled
  • customquenched with ethanol
  • additiondiluted with 10% aqueous potassium carbonate
  • extractionextracted with ethyl acetate
  • dry with materialThe organics were dried over MgSO4
  • concentrationconcentrated to an oil
  • customThe residue was chromatographed on silica gel (70:25:5 CHCl3/EtOAc/MeOH/H2O)
  • 出典と根拠

    ORDレコード
    ord-9fe5baa1f4e44925b48ac668b03ff758
    出典データセット
    uspto-grants-2002_06
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06410526B1

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