6-Methoxynaphthalene-1,2-dione → Tert-butyl 4-hydroxy-4-{[(7-methoxy-3,4-dioxo-3,4-dihydronaphthalen-1-yl)thio]methyl}piperidine-1-carboxylate
반응식
[OH:1][C:2]1([CH2:15][SH:16])[CH2:7][CH2:6][N:5]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[CH2:4][CH2:3]1.[CH3:17][O:18][C:19]1[CH:20]=[C:21]2[C:26](=[CH:27][CH:28]=1)[C:25](=[O:29])[C:24](=[O:30])[CH:23]=[CH:22]2>C(#N)C>[OH:1][C:2]1([CH2:15][S:16][C:22]2[C:21]3[C:26](=[CH:27][CH:28]=[C:19]([O:18][CH3:17])[CH:20]=3)[C:25](=[O:29])[C:24](=[O:30])[CH:23]=2)[CH2:7][CH2:6][N:5]([C:8]([O:10][C:11]([CH3:12])([CH3:13])[CH3:14])=[O:9])[CH2:4][CH2:3]1참가 물질
4
실험 절차
tert-butyl 4-hydroxy-4-{[(7-methoxy-3,4-dioxo-3,4-dihydronaphthalen-1-yl)thio]methyl}piperidine-1-carboxylate was synthesized using tert-butyl 4-hydroxy-4-(mercaptomethyl)piperidine-1-carboxylate, 6-methoxynaphthalene-1,2-dione, acetonitrile as the solvent and conditions outlined in procedure F [step (i)]. The crude intermediate was used in step (ii) without any further purification.
후처리
- customThe crude intermediate was used in step (ii) without any further purification
출처 및 근거
- ORD 기록
- ord-826761078ef041aa93cb837335488809
- 출처 데이터셋
- uspto-grants-2011_10
- 특허 번호
- US08039503B2
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