반응식
Br[C:2]1[CH:3]=[CH:4][C:5]2[C:9]3[CH:10]=[CH:11][C:12](Br)=[CH:13][C:8]=3[S:7](=[O:16])(=[O:15])[C:6]=2[CH:17]=1.[CH2:18]([N:20]([CH2:24][CH3:25])[CH2:21][C:22]#[CH:23])[CH3:19].[CH2:26]([N:28]([CH2:31][CH3:32])[CH2:29][CH3:30])[CH3:27].[CH3:33]N(C=O)C>CCOC(C)=O.Cl[Pd-2](Cl)(P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Cu]I>[CH2:18]([N:20]([CH2:24][CH3:25])[CH2:21][C:22]#[C:23][C:2]1[CH:3]=[CH:4][C:5]2[C:9]3[CH:10]=[CH:11][C:12]([C:33]#[C:27][CH2:26][N:28]([CH2:31][CH3:32])[CH2:29][CH3:30])=[CH:13][C:8]=3[S:7](=[O:16])(=[O:15])[C:6]=2[CH:17]=1)[CH3:19]참가 물질
8
반응물 4
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 65 °C
실험 절차
A mixture of 3,7-dibromodibenzothiophene 5,5-dioxide (0.33 g, 0.88 mmol; see J. Med. Chem. 1978, 21, 1084), 3-diethylamino-1-propyne (0.5 mL, 3.4 mmol; Lancaster), triethylamine (0.6 mL, 4.2 mmol; Acros), dichlorobis(triphenylphosphino)palladium(II) (Cl2Pd(PPh3)2; 25 mg, 0.035 mmol; Aldrich), and copper(I) iodide (38 mg, 0.20 mmol; Aldrich) in DMF (10 mL) was heated to 65° C. for 60 h. The reaction mixture was diluted with EtOAc, washed with water and brine, and dried over Na2SO4. The residue was purified by chromatography (16 g silica gel, 2-7% gradient MeOH in CH2Cl2to afford the title compound (0.31 g, 0.71 mmol, 82% yield): MS (DCl/NH3) m/z 435 (M+H)+.
후처리
- washwashed with water and brine
- dry with materialdried over Na2SO4
- customThe residue was purified by chromatography (16 g silica gel, 2-7% gradient MeOH in CH2Cl2to
출처 및 근거
- ORD 기록
- ord-b40e7644f83343a7a88643ebda83fd87
- 출처 데이터셋
- uspto-grants-2008_04
- 특허 번호
- US07365193B2
연결된 노트
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