Hydrochloric Acid → HCID 178434721、化合物
反応式
[C:1]1([C@H:7]([O:9][C:10](=[O:35])[NH:11][C:12]2[C:13]([CH3:34])=[N:14][O:15][C:16]=2[C:17]2[CH:22]=[CH:21][C:20]([C:23]3[CH:28]=[CH:27][C:26]([C:29]4([C:32]#[N:33])[CH2:31][CH2:30]4)=[CH:25][CH:24]=3)=[CH:19][CH:18]=2)[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CN(C)CCO.Cl.[N-:43]=[N+:44]=[N-:45].[Na+]>COCCOCCOC.C(Cl)Cl.O>[C:1]1([C@H:7]([O:9][C:10](=[O:35])[NH:11][C:12]2[C:13]([CH3:34])=[N:14][O:15][C:16]=2[C:17]2[CH:22]=[CH:21][C:20]([C:23]3[CH:24]=[CH:25][C:26]([C:29]4([C:32]5[NH:45][N:44]=[N:43][N:33]=5)[CH2:30][CH2:31]4)=[CH:27][CH:28]=3)=[CH:19][CH:18]=2)[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 3
実験手順
{5-[4′-(1-Cyano-cyclopropyl)-biphenyl-4-yl]-3-methyl-isoxazol-4-yl}-carbamic acid (R)-1-phenyl-ethyl ester (0.385 g, 0.83 mmol) and N,N-dimethylethanolamine (0.101 mL, 1.0 mmol) were combined in diglyme (diethylene glycol dimethyl ether; 2 mL). Hydrochloric acid (4M in 1,4-dioxane; 4.2 mL) was added, and the reaction was stirred for 15 minutes. Additional N,N-dimethylethanolamine (0.221 mL, 2.2 mmol) was added, followed by sodium azide (0.098 g, 1.5 mmol), and the reaction was stirred at 120° C. for 24 hours. After cooling to room temperature, the mixture was diluted with CH2Cl2 (20 mL) and H2O (10 mL). The organic layer was dried over MgSO4, filtered, and concentrated, and the residue was purified by silica gel chromatography to give the title compound.
後処理
- stirringthe reaction was stirred at 120° C. for 24 hours
- dry with materialThe organic layer was dried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- customthe residue was purified by silica gel chromatography
出典と根拠
- ORDレコード
- ord-c5e73e8e354642dca8412819dbb75e7a
- 出典データセット
- uspto-grants-2012_09
- 特許番号
- US08273780B2
反応ノート
読み込み中…