반응식
O[C:2]1[CH:7]=[CH:6][C:5]2[C:8]3([CH3:22])[CH2:13][CH2:12][N:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:10][CH:9]3[O:21][C:4]=2[CH:3]=1.[OH:23]C1C(OC)=CC=CC=1C(=O)C>>[OH:23][C:7]1[CH:2]=[CH:3][C:4]2[O:21][CH:9]3[CH2:10][N:11]([C:14]([O:16][C:17]([CH3:19])([CH3:20])[CH3:18])=[O:15])[CH2:12][CH2:13][C:8]3([CH3:22])[C:5]=2[CH:6]=1참가 물질
3
실험 절차
Synthesized as described for tert-butyl 7-hydroxy-4a-methyl-3,4,4a,9a-tetrahydro[1]benzofuro[2,3-c]pyridine-2(1H)-carboxylate and as described in J. Med. Chem., 1989, 32, 2221-2226 starting from 1-(2-hydroxy-3-methoxyphenyl)-ethanone. MS m/z 250 [M-tBu+H]+
후처리
- customSynthesized
출처 및 근거
- ORD 기록
- ord-aa31bad2a93b43c88cd7ae72556ca5c1
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08765779B2
연결된 노트
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