반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:17]=[CH:18][C:19]=1[Cl:20])[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([C:13](=[O:16])[CH:14]=O)=[CH:9][CH:8]=1.[CH3:21][O:22][C:23]([C@@H:25]1[CH2:34][C:33]2[C:28](=[CH:29][C:30](O)=[C:31]([NH2:35])[CH:32]=2)[CH2:27][N:26]1[C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38])=[O:24].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(Cl)Cl>ClCCCl.O>[CH3:21][O:22][C:23]([CH:25]1[CH2:34][C:33]2[CH:32]=[C:31]3[C:30]([O:16][C@@H:13]([C:10]4[CH:9]=[CH:8][C:7]([O:6][CH2:5][C:4]5[CH:17]=[CH:18][C:19]([Cl:20])=[C:2]([Cl:1])[CH:3]=5)=[CH:12][CH:11]=4)[CH2:14][NH:35]3)=[CH:29][C:28]=2[CH2:27][N:26]1[C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38])=[O:24]참가 물질
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
[4-(3,4-Dichloro-benzyloxy)-phenyl]-oxo-acetaldehyde (616 mg) was dissolved in DCE (25 mL), and (S)-6-amino-7-hydroxy-3,4-dihydro-1H-isoquinoline-2,3-dicarboxylic acid 2-tert-butyl ester 3-methyl ester (644 mg) and sodium triacetoxyborohydride (520 mg) were added. The mixture was stirred overnight at room temperature. DCM (50 mL) was added to the reaction mixture and poured into water (25 mL). The organic layer was washed with 10% Na2CO3 solution and brine, and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by flash chromatography (hexanes/ethyl acetate from 90:10 to 70:30) to give (S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6,7-dicarboxylic acid 6-tert-butyl ester 7-methyl ester (855 mg).
후처리
- washThe organic layer was washed with 10% Na2CO3 solution and brine
- dry with materialdried over sodium sulfate
- customThe solvent was removed under reduced pressure
- customthe residue was purified by flash chromatography (hexanes/ethyl acetate from 90:10 to 70:30)
출처 및 근거
- ORD 기록
- ord-07c76b50941446a294cb5d682d3a0973
- 출처 데이터셋
- uspto-grants-2013_02
- 특허 번호
- US08383644B2
연결된 노트
불러오는 중…