반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:6](=[O:27])[C:7]3[C:15](=[O:16])[N:14]([C:17]4[CH:22]=[CH:21][C:20]([O:23][CH3:24])=[CH:19][C:18]=4[CH3:25])[N:13]=[C:12]([OH:26])[C:8]=3[NH:9][C:10]=2[CH:11]=1.[CH3:28][NH:29][CH2:30][C@@H:31]([C@H:33]([C@@H:35]([C@@H:37]([CH2:39][OH:40])[OH:38])[OH:36])[OH:34])[OH:32]>CO>[CH3:28][NH:29][CH2:30][C@@H:31]([C@H:33]([C@@H:35]([C@@H:37]([CH2:39][OH:40])[OH:38])[OH:36])[OH:34])[OH:32].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:6](=[O:27])[C:7]3[C:15](=[O:16])[N:14]([C:17]4[CH:22]=[CH:21][C:20]([O:23][CH3:24])=[CH:19][C:18]=4[CH3:25])[N:13]=[C:12]([OH:26])[C:8]=3[NH:9][C:10]=2[CH:11]=1참가 물질
4
실험 절차
7-Chloro-4-hydroxy-2-(4-methoxy-2-methylphenyl)-1,2,5,10-tetrahydropyridazino-[4,5-b]quinoline-1,10-dione (0.45 g, 1.17 mM) was stirred in methanol (20 mL) and N-Methyl-D-Glucamine (0.23 g, 1.17 mM) was added to give a clear yellow solution. This solution was concentrated and the residue was dissolved in water (20 mL) to give a yellow solution. This solution was filtered through a Gellman 0.45 um Acrodisc and concentrated to give a yellow residue. The residue was triturated with 2-propanol (20 mL) to give a yellow suspension. The solids were collected and washed with 2-propanol to give the title compound (0.20 g, 29%) as a yellow powder, mp=177 C (decomp.).
후처리
- customto give a clear yellow solution
- concentrationThis solution was concentrated
- dissolutionthe residue was dissolved in water (20 mL)
- customto give a yellow solution
- filtrationThis solution was filtered through a Gellman 0.45 um Acrodisc
- concentrationconcentrated
- customto give a yellow residue
- customThe residue was triturated with 2-propanol (20 mL)
- customto give a yellow suspension
- customThe solids were collected
- washwashed with 2-propanol
출처 및 근거
- ORD 기록
- ord-462b484e1e1842b99113ed05c8e32d11
- 출처 데이터셋
- uspto-grants-2001_05
- 특허 번호
- US06232313B1
연결된 노트
불러오는 중…