반응식
[CH3:1][C@H:2]([NH2:11])[C@H:3]([OH:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:12][O:13][C:14](=[O:31])[C:15]1[CH:20]=[CH:19][C:18]([N:21]2[C:29]3[C:24](=[CH:25][C:26](I)=[CH:27][CH:28]=3)[CH:23]=[N:22]2)=[CH:17][CH:16]=1.C(=O)([O-])[O-].[Cs+].[Cs+].C(#N)CCC>[Cu]I>[NH2:11][C@@H:2]([CH3:1])[C@@H:3]([C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1)[O:10][C:26]1[CH:25]=[C:24]2[C:29](=[CH:28][CH:27]=1)[N:21]([C:18]1[CH:19]=[CH:20][C:15]([C:14]([O:13][CH3:12])=[O:31])=[CH:16][CH:17]=1)[N:22]=[CH:23]2참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
(1R,2S)-Norephedrine (500 mg, 3.31 mmol), methyl-4-(5-iodoindazole-1-yl)-benzoate (1.28 g, 3.37 mmol), cesiumcarbonate (2.15 g, 6.61 mmol), copper (I)-iodide (314.9 mg, 1.65 mmol) and butyronitrile (2 mL) are stirred in a glass pressure tube at 120° C. for 20 h. The reaction mixture is filtered via a glass microfibre filter, the solvent evaporated and the residue purified by chromatography (silicagel, eluents: dichloromethane/methanol). 217.9 mg (16.4%) of the title compound are obtained.
후처리
- filtrationThe reaction mixture is filtered via a glass microfibre
- filtrationfilter
- customthe solvent evaporated
- customthe residue purified by chromatography (silicagel, eluents: dichloromethane/methanol)
출처 및 근거
- ORD 기록
- ord-a1859bc334c54a22a0996c07c8da5b3b
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07728030B2
연결된 노트
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