反応式
[C:1]1([C:7]2[CH:8]=[CH:9][C:10]3[N:11]([C:13]([CH2:16][C:17]4[CH:18]=[C:19]5[C:24](=[CH:25][CH:26]=4)[N:23]=[CH:22][C:21]([OH:27])=[CH:20]5)=[N:14][N:15]=3)[N:12]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[Na+].Cl.Cl[CH2:32][CH2:33][N:34]([CH3:36])[CH3:35].[OH-].[Na+]>CN(C=O)C>[CH3:35][N:34]([CH3:36])[CH2:33][CH2:32][O:27][C:21]1[CH:22]=[N:23][C:24]2[C:19]([CH:20]=1)=[CH:18][C:17]([CH2:16][C:13]1[N:11]3[N:12]=[C:7]([C:1]4[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=4)[CH:8]=[CH:9][C:10]3=[N:15][N:14]=1)=[CH:26][CH:25]=2参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
6-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinolin-3-ol (0.05 g, 0.1 mmol) was dissolved in DMF (8 mL). SODIUM HYDRIDE (0.01 g, 0.3 mmol) was added and allowed to stir for 1 h at rt. 2-chloro-N,N-dimethylethanamine hydrochloride (0.06 g, 0.4 mmol), which was free-based using 5 N NaOH then extracted with ether, was added. The resulting mixture was continued to stir for 20 h at rt. Solvent was removed in vacuo. The crude material was purified using SiO2 chromatography (Teledyne Isco RediSep®, P/N 68-2203-026, 12 g SiO2, solvent system: DCM:MeOH(2M NH3)=95%:5%, Flow=30 mL/min) to afford the title compound MS m/z: 425.3 (M+H). Calc'd. for C25H24N6O—424.49.
後処理
- extractionthen extracted with ether
- additionwas added
- stirringto stir for 20 h at rt
- customSolvent was removed in vacuo
- customThe crude material was purified
出典と根拠
- ORDレコード
- ord-c7d726a56487461bb65998b96cae2431
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08524900B2
関連ノート
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