Hydrochloric Acid → N-Hydroxy-2-(1H-indol-3-ylacetyl)-1,2,3,4-tetrahydroisoquinoline-7-carboxamide
반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH2:10][C:11]([N:13]2[CH2:22][CH2:21][C:20]3[C:15](=[CH:16][C:17]([C:23]([NH:25][O:26]C4CCCCO4)=[O:24])=[CH:18][CH:19]=3)[CH2:14]2)=[O:12])=[CH:2]1.Cl>CO>[OH:26][NH:25][C:23]([C:17]1[CH:16]=[C:15]2[C:20]([CH2:21][CH2:22][N:13]([C:11](=[O:12])[CH2:10][C:3]3[C:4]4[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=4)[NH:1][CH:2]=3)[CH2:14]2)=[CH:19][CH:18]=1)=[O:24]참가 물질
4
실험 절차
A mixture of 180 mg 2-(1H-indol-3-ylacetyl)-N-(tetrahydro-2H-pyran-2-yloxy)-1,2,3,4-tetrahydroisoquinoline-7-carboxamide, 6 ml methanol and 6 ml 0.1 N aqueous hydrochloric acid are stirred at ambient temperature overnight. The reaction mixture is evaporated and the residue is dissolved in a mixture of acetonitrile and water and lyophilized. 92 mg of the title compound are obtained. MH+=350.0
후처리
- customThe reaction mixture is evaporated
- dissolutionthe residue is dissolved in a mixture of acetonitrile and water
출처 및 근거
- ORD 기록
- ord-94c189c322b34180bbd0b7e10befd700
- 출처 데이터셋
- uspto-grants-2013_11
- 특허 번호
- US08575193B2
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