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2-Aminoquinoline → 3-{3,5-dimethyl-4-[6-(quinolin-2-ylcarbamoyl)-1H-indol-2-yl]-phenyl}-propionic acid methyl ester

HRID 1514957
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HRID 1514957 반응식
[CH3:1][O:2][C:3]([CH2:5][CH2:6][C:7]1[CH:12]=[C:11]([CH3:13])[C:10]([C:14]2[NH:15][C:16]3[C:21]([CH:22]=2)=[CH:20][CH:19]=[C:18]([C:23]([OH:25])=O)[CH:17]=3)=[C:9]([CH3:26])[CH:8]=1)=[O:4].[NH2:27][C:28]1[CH:37]=[CH:36][C:35]2[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=2)[N:29]=1.CCN=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1.[I-].C[NH+]1CCN(CCC)C1>C1COCC1.C(OCC)(=O)C>[CH3:1][O:2][C:3](=[O:4])[CH2:5][CH2:6][C:7]1[CH:8]=[C:9]([CH3:26])[C:10]([C:14]2[NH:15][C:16]3[C:21]([CH:22]=2)=[CH:20][CH:19]=[C:18]([C:23](=[O:25])[NH:27][C:28]2[CH:37]=[CH:36][C:35]4[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=4)[N:29]=2)[CH:17]=3)=[C:11]([CH3:13])[CH:12]=1
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참가 물질

8

반응물 5

HCID 113792-AminoquinolineHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 669660741-Methyl-3-propylimidazolinium iodideHCID 669662052-[4-(2-Methoxycarbonylethyl)-2,6-dimethylphenyl]-1H-indole-6-carboxylic acid

생성물 1

HCID 66965694
3-{3,5-dimethyl-4-[6-(quinolin-2-ylcarbamoyl)-1H-indol-2-yl]-phenyl}-propionic acid methyl ester

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 8857Ethyl Acetate용매

반응 조건

온도
150 °C

실험 절차

A mixture of 2-[4-(2-methoxycarbonylethyl)-2,6-dimethylphenyl]-1H-indole-6-carboxylic acid (600 mg, 1.71 mmol), 2-aminoquinoline (246 mg, 1.71 mmol), EDCI (491 mg, 2.56 mmol), HOBT (254 mg, 1.88 mmol) and 1-methyl-3-propylimidazolinium iodide (140 mg, 560 μmol) in THF (10 mL) was heated in a microwave apparatus at 150° C. for 3 h then the mixture was poured into ethyl acetate and extracted with water twice and brine once. The ethyl acetate layer was dried, filtered, and removed under reduced pressure, and the residual material was chromatographed using a 20-50% gradient of heptane/ethyl acetate to afford 3-{3,5-dimethyl-4-[6-(quinolin-2-ylcarbamoyl)-1H-indol-2-yl]-phenyl}-propionic acid methyl ester. 1H NMR (DMSO-d6, 400 MHz): δ 11.56 (s, 1H), 11.00 (s, 1H), 8.39 (s, 2H), 8.16 (s, 1H), 7.95 (d, J=7.4 Hz, 1H), 7.88 (d, J=8.3 Hz, 1H), 7.79 (dd, J=8.3, 1.5 Hz, 1H), 7.73 (TD, J=7.0, 1.4 Hz, 1H), 7.63 (d, J=8.3 Hz, 1H), 7.52 (t, J=7.0 Hz, 1H), 7.05 (s, 2H), 6.41 (d, J=1.3 Hz, 1H), 3.62 (s, 3H), 2.85 (t, J=7.4 Hz, 2H), 2.67 (t, J=7.4 Hz, 2H), 2.12 (s, 6H). MS (m/z) 478.2 (M+1); Retention time=1.58 min (Method 10).

후처리

  1. extractionextracted with water twice
  2. dry with materialThe ethyl acetate layer was dried
  3. filtrationfiltered
  4. customremoved under reduced pressure
  5. customthe residual material was chromatographed

출처 및 근거

ORD 기록
ord-8b9f846e892f4cb9aad681cff2ea7e13
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08222248B2

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