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Hydrochloric Acid → 5,6-dihydro-2-(2-phenylethyl)-4H-imidazo[4,5,1-ij]quinoline

HRID 341833
ノート
印刷プレビュー

反応式

HRID 341833 の反応式
[NH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[NH:10][CH2:9][CH2:8][CH2:7]2.[C:12]1([CH2:18][CH2:19][CH:20]=O)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.Cl>CO>[C:12]1([CH2:18][CH2:19][C:20]2[N:10]3[C:11]4[C:6]([CH2:7][CH2:8][CH2:9]3)=[CH:5][CH:4]=[CH:3][C:2]=4[N:1]=2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=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 313Hydrochloric AcidHCID 7707BenzenepropanalHCID 1046728-Quinolinamine, 1,2,3,4-tetrahydro-

生成物 1

HCID 158384635,6-dihydro-2-(2-phenylethyl)-4H-imidazo[4,5,1-ij]quinoline

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Thirty-five grams of 8-amino-1,2,3,4-tetrahydroquinoline was dissolved in methanol (700 mL) and, following the addition of 3-phenylpropionaldehyde (37.4 mL) and 1N HCl (7 mL) and subsequent stirring at room temperature for 1 hr, silica gel (75 g) was added to the reaction solution and the solvent was removed under reduced pressure. The residue was heated at 100° C. for 1 hr, purified by silica gel column chromatography (eluent: dichloromethane/ethyl acetate) and recrystallized with ethyl acetate to yield the titled compound as pale yellow crystals (19.3 g).

後処理

  1. additionsilica gel (75 g) was added to the reaction solution
  2. customthe solvent was removed under reduced pressure
  3. temperatureThe residue was heated at 100° C. for 1 hr
  4. custompurified by silica gel column chromatography (eluent: dichloromethane/ethyl acetate)
  5. customrecrystallized with ethyl acetate

出典と根拠

ORDレコード
ord-73f3c5abdc1a498c9e54f3864ff76f44
出典データセット
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05856334

反応ノート

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