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p-Toluenesulfonic acid → 1-Methyl-5-[2-(4-trifluoromethyl-phenyl)-ethylamino]-5,6,7,8-tetrahydro-1H-quinolin-2-one

HRID 1195172
ノート
印刷プレビュー

反応式

HRID 1195172 の反応式
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][NH2:11])=[CH:5][CH:4]=1.[CH3:14][N:15]1[C:24]2[CH2:23][CH2:22][CH2:21][C:20](=O)[C:19]=2[CH:18]=[CH:17][C:16]1=[O:26].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[F:1][C:2]([F:12])([F:13])[C:3]1[CH:4]=[CH:5][C:6]([CH2:9][CH2:10][NH:11][CH:20]2[CH2:21][CH2:22][CH2:23][C:24]3[N:15]([CH3:14])[C:16](=[O:26])[CH:17]=[CH:18][C:19]2=3)=[CH:7][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6101p-Toluenesulfonic acidHCID 19881062-[4-(Trifluoromethyl)phenyl]ethan-1-amineHCID 104422421-Methyl-7,8-dihydroquinoline-2,5(1H,6H)-dione

生成物 1

HCID 103379341-Methyl-5-[2-(4-trifluoromethyl-phenyl)-ethylamino]-5,6,7,8-tetrahydro-1H-quinolin-2-one収率 65%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A mixture of 2-(4-trifluoromethylphenyl)ethylamine (4.1 g), 5,6,7,8-tetrahydro-1-methyl-5oxo-2(1H)-quinolinone (3.0 g), and para-toluenesulfonic acid (256 mg) was heated in refluxing toluene (50 ml), with azeotropic removal or water, for 40 hrs. An additional 2.0 g of the amine was added and the mixture was refluxed for 36 hr. The solution was cooled, and the mixture was concentrated in vacuo. Sodium borohydride (0.6 g) was added to a solution of the residue in ethyl alcohol (50 ml), and the resulting mixture was stirred at room temperature for 1 hr. The mixture was concentrated in vacuo, the residue was quenched with water, and the mixture was extracted with dichloromethane. The combined organic layers were washed with brine, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated. The residue was recrystallized from ethyl acetate/hexanes to provide, in two crops, 3.8 g (65%) of product, mp 104°-106° C.

後処理

  1. temperaturewas heated
  2. customwith azeotropic removal or water
  3. additionAn additional 2.0 g of the amine was added
  4. temperaturethe mixture was refluxed for 36 hr
  5. temperatureThe solution was cooled
  6. concentrationthe mixture was concentrated in vacuo
  7. additionSodium borohydride (0.6 g) was added to a solution of the residue in ethyl alcohol (50 ml)
  8. concentrationThe mixture was concentrated in vacuo
  9. customthe residue was quenched with water
  10. extractionthe mixture was extracted with dichloromethane
  11. washThe combined organic layers were washed with brine
  12. dry with materialdried over anhydrous magnesium sulfate
  13. filtrationfiltered
  14. concentrationthe filtrate was concentrated
  15. customThe residue was recrystallized from ethyl acetate/hexanes

出典と根拠

ORDレコード
ord-0bc2d6547f514ef3b9ef0903c9b4a9eb
出典データセット
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05110815

反応ノート

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