Triethylamine → 3-ethoxy-4-{[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl)amino}-3-cyclobutene-1,2-dione
反応式
[CH3:1][N:2]1[C:6]([NH:7][C:8]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[C:5]([NH2:27])[CH:4]=[N:3]1.C(N(CC)CC)C.[CH3:35][CH2:36][O:37][C:38]1[C:42](=O)[C:40](=[O:41])[C:39]=1[O:44]CC.C(OCC)(=O)C>C(O)C.CCCCCC>[CH2:36]([O:37][C:38]1[C:39](=[O:44])[C:40](=[O:41])[C:42]=1[NH:27][C:5]1[CH:4]=[N:3][N:2]([CH3:1])[C:6]=1[NH:7][C:8]([C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1)([C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH3:35]参加物
7
実験手順
To a suspension of 1-methyl-N5-trityl-1H-pyrazole-4,5-diamine 1.60 g) in ethanol (50 ml) were added triethylamine (0.627 ml) and diethyl squarate (0.858 ml), and the mixture was stirred at room temperature for 22 hours. To the reaction mixture were added ethyl acetate (200 ml) and hexane (100 ml), and the solution was washed successively with water, 5% aqueous citric acid solution and brine. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crystalline residue was washed with diethyl ether and dried in vacuo to give 3-ethoxy-4-{[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]amino}-3-cyclobutene-1,2-dione (1.45 g) as a solid.
後処理
- washthe solution was washed successively with water, 5% aqueous citric acid solution and brine
- dry with materialThe organic layer was dried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- washThe crystalline residue was washed with diethyl ether
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-b2a04be7d9da44ce801bfd7ee17385cb
- 出典データセット
- uspto-grants-2007_03
- 特許番号
- US07192943B2
反応ノート
読み込み中…