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

HRID 341833
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HRID 341833 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 7707BenzenepropanalHCID 1046728-Quinolinamine, 1,2,3,4-tetrahydro-

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-73f3c5abdc1a498c9e54f3864ff76f44
출처 데이터셋
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05856334

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