Triethylamine → 5-(2,6-Dichloro-3,5-dimethoxy-phenyl)-quinoline-8-carboxylic acid [4-(4-ethyl-piperazin-1-yl)-phenyl]-amide

HRID 43191

반응식

HRID 43191 반응식
CCCP(=O)=O.[Cl:7][C:8]1[C:13]([O:14][CH3:15])=[CH:12][C:11]([O:16][CH3:17])=[C:10]([Cl:18])[C:9]=1[C:19]1[CH:28]=[CH:27][C:26]([C:29](O)=[O:30])=[C:25]2[C:20]=1[CH:21]=[CH:22][CH:23]=[N:24]2.[CH2:32]([N:34]1[CH2:39][CH2:38][N:37]([C:40]2[CH:46]=[CH:45][C:43]([NH2:44])=[CH:42][CH:41]=2)[CH2:36][CH2:35]1)[CH3:33].CCN(CC)CC>CN(C1C=CN=CC=1)C.CN(C=O)C.CCOC(C)=O.O>[CH2:32]([N:34]1[CH2:35][CH2:36][N:37]([C:40]2[CH:46]=[CH:45][C:43]([NH:44][C:29]([C:26]3[CH:27]=[CH:28][C:19]([C:9]4[C:10]([Cl:18])=[C:11]([O:16][CH3:17])[CH:12]=[C:13]([O:14][CH3:15])[C:8]=4[Cl:7])=[C:20]4[C:25]=3[N:24]=[CH:23][CH:22]=[CH:21]4)=[O:30])=[CH:42][CH:41]=2)[CH2:38][CH2:39]1)[CH3:33]

참가 물질

9

실험 절차

A mixture of propylphosphonic anhydride (50% in DMF, 0.41 mL, 0.70 mmol, 2 equiv), 5-(2,6-dichloro-3,5-dimethoxy-phenyl)-quinoline-8-carboxylic acid (Step 159.1) (132 mg, 0.35 mmol), 4-(4-ethylpiperazin-1-yl)-aniline (Step 1.9) (79 mg, 0.39 mmol, 1.1 equiv), DMAP (3 mg), and Et3N (0.49 mL, 3.5 mmol, 10 equiv) in DMF (3 mL), was stirred for 16 h at rt, under an argon atmosphere. The reaction mixture was diluted with EtOAc and H2O. The aqueous layer was separated and extracted with EtOAc. The combined organic phase was washed with brine, dried (Na2SO4), filtered and concentrated. The residue was purified by trituration in EtOAc to afford the title compound as a yellow solid: ES-MS: 564.9/566.9 [M+H]+; ta=4.45 min (System 1).

후처리

  1. customThe aqueous layer was separated
  2. extractionextracted with EtOAc
  3. washThe combined organic phase was washed with brine
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was purified by trituration in EtOAc

출처 및 근거

ORD 기록
ord-a2dc595ec5894b4bb60b67f794f6ef20
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08536175B2

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