Acetic Acid → 2-(4-Cyano-benzyl)-3-hydroxy-7,8,9,10-tetrahydro-benzo[h]quinoline-4-carboxylic Acid

HRID 2375574노트

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HRID 2375574 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]3[CH2:13][CH2:12][CH2:11][CH2:10][C:8]3=2)[C:3](=O)[C:2]1=[O:15].[C:16]([C:18]1[CH:23]=[CH:22][C:21]([CH2:24][C:25](=O)COC(=O)C)=[CH:20][CH:19]=1)#[N:17].[C:32]([OH:35])(=[O:34])C>C(O)C.[OH-].[Na+]>[C:16]([C:18]1[CH:23]=[CH:22][C:21]([CH2:24][C:25]2[C:2]([OH:15])=[C:3]([C:32]([OH:35])=[O:34])[C:4]3[C:9](=[C:8]4[CH2:10][CH2:11][CH2:12][CH2:13][C:7]4=[CH:6][CH:5]=3)[N:1]=2)=[CH:20][CH:19]=1)#[N:17]

참가 물질

6

실험 절차

In a 25 mL round-bottomed flask, 6,7,8,9-tetrahydrobenzo[g]indoline-2,3-dione (0.119 g, 0.590 mmol) was taken up in 1 mL ethanol and 3 mL 10 M NaOH, and the mixture heated at reflux temperature for 3 minutes. A solution of acetic acid 3-(4-cyano-phenyl)-2-oxo-propyl ester (0.167 g, 0.767 mmol) in 3 mL ethanol was then added and the reaction further heated for 10 minutes. The reaction mixture was then cooled to room temperature and acidified with glacial acetic acid, and the yellow precipitate collected by filtration. The procedure described above for the purification of example 7 was followed. Product was obtained as a bright yellow powder (42 mg, 20% yield): 1H NMR (400 MHz, DMSO-D6) δ ppm 1.74-1.87 (m, 4H) 2.83 (t, J=5.31 Hz, 2H) 3.12 (t, J=5.43 Hz, 2H), 4.40 (s, 2H), 7.28 (d, J=9.09 Hz, 1H) 7.51 (d, J=8.59 Hz, 2H) 7.75 (d, J=8.34 Hz, 2H) 8.23 (d, J=8.84 Hz, 1H).

후처리

  1. temperatureat reflux temperature for 3 minutes
  2. customthe reaction
  3. temperaturefurther heated for 10 minutes
  4. filtrationthe yellow precipitate collected by filtration
  5. customThe procedure described above for the purification of example 7

출처 및 근거

ORD 기록
ord-54a8668a1b9d4c40a3b9f49b26c10368
출처 데이터셋
uspto-grants-2008_12
특허 번호
US07465798B2

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