Sodium Bicarbonate → N-Benzyl-N-[2-benzyloxy-5-(2-bromoacetyl)phenyl]methanesulfonamide
반응식
[Br-:1].[Br-].[Br-].C1([N+](C)(C)C)C=CC=CC=1.C1([N+](C)(C)C)C=CC=CC=1.C1([N+](C)(C)C)C=CC=CC=1.[C:34]([C:37]1[CH:38]=[CH:39][C:40]([O:55][CH2:56][C:57]2[CH:62]=[CH:61][CH:60]=[CH:59][CH:58]=2)=[C:41]([N:43]([CH2:48][C:49]2[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=2)[S:44]([CH3:47])(=[O:46])=[O:45])[CH:42]=1)(=[O:36])[CH3:35].C(=O)(O)[O-].[Na+]>C1COCC1>[CH2:48]([N:43]([C:41]1[CH:42]=[C:37]([C:34](=[O:36])[CH2:35][Br:1])[CH:38]=[CH:39][C:40]=1[O:55][CH2:56][C:57]1[CH:58]=[CH:59][CH:60]=[CH:61][CH:62]=1)[S:44]([CH3:47])(=[O:46])=[O:45])[C:49]1[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=1참가 물질
실험 절차
Phenyltrimethylammonium tribromide (1.19 g, 3.16 mmol) was added to a solution of N-(5-acetyl-2-benzyloxyphenyl)-N-benzylmethanesulfonamide (32) (1.23 g, 3.01 mmol) in anhydrous THF (15 mL) in three portions. The reaction mixture was stirred at rt for 16 h. An aqueous sodium bicarbonate solution (5%, 15 mL) was then added. The mixture was extracted with dichloromethane and combined organics were concentrated by rotary evaporation. The resulting residue was purified by Biotage silica gel column chromatography eluting with dichloromethane to give bromo ketone 33 as a solid (1.25 g, 85% yield): 1H NMR (500 MHz, CDCl3) δ 2.85 (s, 3H), 4.21 (s, 2H), 4.75 (br, 2H), 5.19 (s, 2H), 7.08 (d, 1H), 7.22 (m, 5H), 7.43 (m, 5H), 7.65 (d, 1H), 7.92 (dd, 1H).
후처리
- extractionThe mixture was extracted with dichloromethane
- concentrationcombined organics were concentrated by rotary evaporation
- customThe resulting residue was purified by Biotage silica gel column chromatography
- washeluting with dichloromethane
출처 및 근거
- ORD 기록
- ord-9879d8b0080e468983b71eab37cd290a
- 출처 데이터셋
- uspto-grants-2012_04
- 특허 번호
- US08163758B2
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