Hydrochloric Acid → Pyridine, 2-(4-aminopyrazol-1-yl)-
反応式
C(OC(=O)[NH:7][C:8]1[CH:9]=[N:10][N:11]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=2)[CH:12]=1)(C)(C)C.Cl.[OH-].[Na+]>O1CCOCC1>[N:14]1[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=1[N:11]1[CH:12]=[C:8]([NH2:7])[CH:9]=[N:10]1参加物
5
実験手順
A solution of (1-pyridin-2-yl-1H-pyrazol-4-yl)-carbamic acid tert-butyl ester (185 mg, 0.72 mmol) in dioxane (1.85 ml) was treated with 4M HCl in dioxane (1.85 ml) and the resulting suspension was stirred at ambient temperature for 2 hours. The reaction mixture was adjusted to basic pH with sodium hydroxide (20 ml, 0.5M aqueous solution) and extracted with dichloromethane. The combined organic phases were dried and the solvent was evaporated to yield the product as light brown solid (110 mg, 96%) which was used without any further purification. MS: M=161.3 (M+H)+
後処理
- extractionextracted with dichloromethane
- customThe combined organic phases were dried
- customthe solvent was evaporated
出典と根拠
- ORDレコード
- ord-9fd12c0b204e4bd3b2985134fb0f058c
- 出典データセット
- uspto-grants-2013_06
- 特許番号
- US08470820B2
反応ノート
読み込み中…