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Ethyl 3-(2,4-diaminophenyl)propanoate → 7-amino-3,4-dihydro-1H-quinolin-2-one

HRID 519075
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HRID 519075 반응식
[NH2:1][C:2]1[CH:7]=[C:6]([NH2:8])[CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10][C:11]([O:13]CC)=O>CCO>[NH2:8][C:6]1[CH:7]=[C:2]2[C:3]([CH2:9][CH2:10][C:11](=[O:13])[NH:1]2)=[CH:4][CH:5]=1
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참가 물질

3

반응물 1

HCID 67287969Ethyl 3-(2,4-diaminophenyl)propanoate

생성물 1

HCID 52002427-amino-3,4-dihydro-1H-quinolin-2-one수율 87%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A suspension of Pd(OH)2/C (10%, 3.0 g) and (E)-ethyl 3-(2,4-dinitrophenyl)acrylate (12.0 g, 45.1 mmol) in MeOH (80 mL) was stirred at 25° C. under an atmosphere of H2 (45 psi) for 15 h. The mixture was filtered and the filtrate was concentrated in vacuo to give 3-(2,4-diamino-phenyl)-propionic acid ethyl ester (8.6 g, 98%), which was used directly in the next step without further purification. A solution of ethyl 3-(2,4-diaminophenyl)propanoate (8.6 g, 41.3 mmol) in EtOH (50 mL) was stirred at 85-100° C. for 48 h. The reaction mixture was cooled to ambient temperature and the solvent was removed in vacuo. EtOAc (10 mL) was added to the residue and the precipitate was collected by filtration to give 7-amino-3,4-dihydro-1H-quinolin-2-one (5.8 g, 87%). 1H NMR (DMSO-d6, 400 MHz): δ 9.83 (brs, 1H), 6.76 (d, J=7.6 Hz, 1H), 6.12 (m, 2H), 4.95 (brs, 2H), 2.65 (t, J=7.2 Hz, 2H), 2.36 (t, J=7.2 Hz, 2H).

후처리

  1. customwas used directly in the next step without further purification
  2. customthe solvent was removed in vacuo
  3. additionEtOAc (10 mL) was added to the residue
  4. filtrationthe precipitate was collected by filtration

출처 및 근거

ORD 기록
ord-4ac59ab371dd485e87ae82dc82e9704b
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115151B2

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