Potassium Iodide → Ammonia

HRID 1433266노트

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HRID 1433266 반응식
[CH2:1]([O:8][C:9]1[CH:10]=[CH:11][C:12]([C@@H:20]([O:23][Si:24]([C:27]([CH3:30])([CH3:29])[CH3:28])([CH3:26])[CH3:25])[CH2:21]Br)=[C:13]2[C:18]=1[NH:17][C:16](=[O:19])[CH:15]=[CH:14]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.Cl.[NH2:33][CH2:34][CH2:35][C:36]1[CH:69]=[CH:68][C:39]([O:40][CH2:41][CH2:42][CH2:43][CH2:44][C:45]2[CH:50]=[CH:49][C:48]([OH:51])=[C:47]([C@@H:52]([C:62]3[CH:67]=[CH:66][CH:65]=[CH:64][CH:63]=3)[CH2:53][CH2:54][N:55]([CH:59]([CH3:61])[CH3:60])[CH:56]([CH3:58])[CH3:57])[CH:46]=2)=[CH:38][CH:37]=1.C(=O)([O-])O.[Na+].[I-].[K+].C(#N)CC>C(OCC)(=O)C>[NH3:17].[CH2:1]([O:8][C:9]1[CH:10]=[CH:11][C:12]([C@@H:20]([O:23][Si:24]([C:27]([CH3:30])([CH3:29])[CH3:28])([CH3:26])[CH3:25])[CH2:21][NH:33][CH2:34][CH2:35][C:36]2[CH:37]=[CH:38][C:39]([O:40][CH2:41][CH2:42][CH2:43][CH2:44][C:45]3[CH:50]=[CH:49][C:48]([OH:51])=[C:47]([C@@H:52]([C:62]4[CH:63]=[CH:64][CH:65]=[CH:66][CH:67]=4)[CH2:53][CH2:54][N:55]([CH:56]([CH3:58])[CH3:57])[CH:59]([CH3:60])[CH3:61])[CH:46]=3)=[CH:68][CH:69]=2)=[C:13]2[C:18]=1[NH:17][C:16](=[O:19])[CH:15]=[CH:14]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

8

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온도
90 °C

실험 절차

8-(benzyloxy)-5-[(1R)-2-bromo-1-{[tert-butyl(dimethyl)silyl]oxy}ethyl]quinolin-2(1H)-one (Prepared according to WO2005/092861, 530 mg, 1.1 mmol), 4-{4-[4-(2-aminoethyl)phenoxy]butyl}-2-[(1R)-3-(diisopropylamino)-1-phenylpropyl]phenol bis hydrochloride salt (Preparation 13, 650 mg, 1.3 mmol), sodium hydrogen carbonate (550 mg, 6.5 mmol) and potassium iodide (50 mg, 0.30 mmol) were added to propionitrile (8 ml) and heated to 90° C. and left to stir overnight. After cooling, ethyl acetate and saturated aqueous sodium hydrogen carbonate were added, organics separated and washed with more saturated aqueous sodium hydrogen carbonate, then brine and then dried (magnesium sulphate) and solvent removed in vacuo. The residue was purified by column chromatography on silica gel eluting with dichloromethane:methanol:880 ammonia (100/0/0 to 94/6/0.6 by volume) to furnish the title compound as an oil, 406 mg.

후처리

  1. waitleft
  2. temperatureAfter cooling
  3. customorganics separated
  4. washwashed with more saturated aqueous sodium hydrogen carbonate
  5. dry with materialbrine and then dried (magnesium sulphate) and solvent
  6. customremoved in vacuo
  7. customThe residue was purified by column chromatography on silica gel eluting with dichloromethane

출처 및 근거

ORD 기록
ord-4273ec02a0d347c9a693aa8f543baae3
출처 데이터셋
uspto-grants-2009_11
특허 번호
US07612084B2

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