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SMR000102306 → 1H-Cyclopenta(b)quinoline, 2,3-dihydro-9-amino-7-bromo-

HRID 366395
ノート
印刷プレビュー

反応式

HRID 366395 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[CH2:13][CH2:12][CH2:11][C:10]=2[C:14]#[N:15])=[CH:4][CH:3]=1>[Ti](Cl)(Cl)(Cl)Cl.[OH-].[Na+]>[NH2:15][C:14]1[C:4]2[CH:3]=[C:2]([Br:1])[CH:7]=[CH:6][C:5]=2[N:8]=[C:9]2[CH2:13][CH2:12][CH2:11][C:10]=12
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 622051SMR000102306

生成物 1

HCID 30413501H-Cyclopenta(b)quinoline, 2,3-dihydro-9-amino-7-bromo-

試薬・触媒・溶媒 2

HCID 24193Titanium Tetrachloride触媒HCID 14798Sodium Hydroxide溶媒

反応条件

温度
140 °C

実験手順

Under nitrogen, titanium tetrachloride (1.2 ml, 11 mmol) was added to the above enamine (Example 22) (2.6 g, 20 mmol) and the stirred mixture was heated at 140° C. for 1 hour. After cooling, 10M-sodium hydroxide solution (20 ml) was added and the mixture heated under reflux for 1 hour. After being allowed to cool, this mixture was filtered and the solids washed with dichloromethane. Any organics in the filtrate were also extracted into dichloromethane. All extracts were combined, dried (Na2SO4), filtered and the solvent evaporated. Kugelrohr distillation (180° C., 0.04 mmHg) gave the product as a pale yellow powder.

後処理

  1. temperatureAfter cooling
  2. temperaturethe mixture heated
  3. temperatureunder reflux for 1 hour
  4. temperatureto cool
  5. filtrationthis mixture was filtered
  6. washthe solids washed with dichloromethane
  7. extractionAny organics in the filtrate were also extracted into dichloromethane
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. customthe solvent evaporated
  11. distillationKugelrohr distillation (180° C., 0.04 mmHg)

出典と根拠

ORDレコード
ord-2e4ec425ea4c498ab9a30c28042701d1
出典データセット
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06130228

反応ノート

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