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HCID 70255947、化合物 → 7-Fluoro-2,3-dihydro-1H-cyclopenta[b]quinolin-9-amine

HRID 366393
ノート
印刷プレビュー

反応式

HRID 366393 の反応式
[F: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]([F: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 70255947HCID 70255947、化合物

生成物 1

HCID 232898317-Fluoro-2,3-dihydro-1H-cyclopenta[b]quinolin-9-amine

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 20) (2.0 g, 10 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 (175° C., 0.05 mmHg) gave the product as an off-white 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 (175° C., 0.05 mmHg)

出典と根拠

ORDレコード
ord-7560a5182b6b48c4a429d23fadffba43
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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