反応式
CN([CH:4]=[C:5]1[C:10](=O)[CH2:9][CH2:8][N:7]([C:12]2[CH:17]=[C:16]([N+:18]([O-:20])=[O:19])[CH:15]=[CH:14][C:13]=2[CH3:21])[CH2:6]1)C.[CH3:22][N:23]1[CH2:28][CH2:27][N:26]([C:29]2[CH:34]=[CH:33][C:32]([NH:35][C:36]([NH2:38])=[NH:37])=[CH:31][CH:30]=2)[CH2:25][CH2:24]1.C([O-])(=O)C.[Na+]>C(O)C.O>[CH3:21][C:13]1[CH:14]=[CH:15][C:16]([N+:18]([O-:20])=[O:19])=[CH:17][C:12]=1[N:7]1[CH2:8][CH2:9][C:10]2[N:37]=[C:36]([NH:35][C:32]3[CH:31]=[CH:30][C:29]([N:26]4[CH2:27][CH2:28][N:23]([CH3:22])[CH2:24][CH2:25]4)=[CH:34][CH:33]=3)[N:38]=[CH:4][C:5]=2[CH2:6]1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of 3-Dimethylaminomethylene-1-(2-methyl-5-nitrophenyl)-piperidin-4-one (12.06 gm, 41.7 mmol)[as prepared in reference 1] in Ethanol (250 ml) were added N-[4-(4-Methyl-piperazin-1-yl)-phenyl]-guanidine (38.9 gm, 167 mmol) and sodium acetate (27.32 gm, 334 mmol) and solution was heated under reflux for 12 hours. After cooling to room temperature, the reaction mixture was diluted with water, extracted with ethyl acetate. The organic layer was washed with brine, dried [sodium sulfate] and concentrated under vacuum. The crude product obtained was further purified by silica gel chromatography using 5-10% Methanol/Chloroform as eluent to give pure desired product [47] i.e., [6-(2-Methyl-5-nitro-phenyl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-2-yl]-[4-(4-methyl-piperazin-1-yl)-phenyl]-amine as yellow solid. (Yield: 3.65 gm, 19.0%).
後処理
- temperaturewas heated
- temperatureunder reflux for 12 hours
- extractionextracted with ethyl acetate
- washThe organic layer was washed with brine
- dry with materialdried [sodium sulfate]
- concentrationconcentrated under vacuum
- customThe crude product obtained
- customwas further purified by silica gel chromatography
出典と根拠
- ORDレコード
- ord-cb10d4bf5efb4a6e97b20e7f3b19818a
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08962637B2
関連ノート
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