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

HRID 993245
ノート
印刷プレビュー

反応式

HRID 993245 の反応式
[NH2:1][CH2:2][CH2:3][CH2:4][C:5]1[N:10]=[CH:9][C:8]([CH2:11][CH2:12][CH2:13][CH2:14][NH2:15])=[CH:7][CH:6]=1.[H-].[Na+]>>[N:10]1[C:9]2[NH:15][CH2:14][CH2:13][CH2:12][CH2:11][C:8]=2[CH:7]=[CH:6][C:5]=1[CH2:4][CH2:3][CH2:2][NH2:1]
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 184089864-[6-(3-Amino-propyl)-pyridin-3-yl]-butyl amine

生成物 1

HCID 184089753-(6,7,8,9-Tetrahydro-5H-pyrido[2,3-b]azepin-2-yl)-propylamine収率 26.9%

実験手順

A mixture of 3-5 (3.0 g, 14.5 mmol) and NaH (1.7 g of a 60% weight dispersion in mineral oil, 47 mmol) in xylenes (100 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 (15:10:1:1 EtOAc/EtOH/NH4OH/H2O) to give 800 mg of 3-6 as a yellow oil.

後処理

  1. customwas purged with argon for 30 min
  2. temperatureheated
  3. temperatureat reflux for 72 hours
  4. temperatureThe mixture was cooled
  5. customquenched with ethanol
  6. additiondiluted with 10% aqueous potassium carbonate
  7. extractionextracted with ethyl acetate
  8. dry with materialThe organics were dried over MgSO4
  9. concentrationconcentrated to an oil
  10. customThe residue was chromatographed on silica gel (15:10:1:1 EtOAc/EtOH/NH4OH/H2O)

出典と根拠

ORDレコード
ord-60ab0d9af6e24d1ea734ca09ee3fe36f
出典データセット
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06472403B2

反応ノート

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