4-tert-Butylphenylboronic acid → 6-(4-tert-butyl-phenoxy)-3,4-dihydro-1H-isoquinoline-2,3-dicarboxylic acid 2-tert-butyl ester 3-methyl ester
반응식
[CH3:1][O:2][C:3]([CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[C:11]([OH:15])[CH:12]=2)[CH2:7][N:6]1[C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])=[O:4].[C:23]([C:27]1[CH:32]=[CH:31][C:30](B(O)O)=[CH:29][CH:28]=1)([CH3:26])([CH3:25])[CH3:24]>C(Cl)Cl.C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[CH3:1][O:2][C:3]([CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[C:11]([O:15][C:30]3[CH:31]=[CH:32][C:27]([C:23]([CH3:26])([CH3:25])[CH3:24])=[CH:28][CH:29]=3)[CH:12]=2)[CH2:7][N:6]1[C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])=[O:4]참가 물질
5
반응물 2
생성물 1
시약·촉매·용매 2
실험 절차
6-Hydroxy-3,4-dihydro-1H-isoquinoline-2,3-dicarboxylic acid 2-tert-butyl ester 3-methyl ester (0.5 g, 1.62 mmol) in DCM (15 mL) was treated with copper acetate (0.59 g, 3.3 mmol), 4-tert-butylphenylboronic acid (0.87 g, 4.8 mmol), and TEA (1.0 mL, 7.9 mmol) by the general procedure G. The crude product was purified by flash column chromatography on silica gel using Hexanes:EtOAc (70:30) to give 0.35 g of 6-(4-tert-butyl-phenoxy)-3,4-dihydro-1H-isoquinoline-2,3-dicarboxylic acid 2-tert-butyl ester 3-methyl ester which was deprotected using general procedure N to give 6-(4-tert-butyl-phenoxy)-1,2,3,4-tetrahydro-isoquinoline-(3S)-carboxylic acid methyl ester hydrochloride salt (0.27 g).
후처리
- customThe crude product was purified by flash column chromatography on silica gel
출처 및 근거
- ORD 기록
- ord-1c8da13226994f1c917c23e88313c587
- 출처 데이터셋
- uspto-grants-2009_06
- 특허 번호
- US07544699B2
반응 노트
불러오는 중…