Water → Hydrochloric Acid
反応式
[CH:1]1([NH:7][C:8]([C:10]2[N:14]=[CH:13][N:12]([CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[N:11]=2)=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[H-].[H-].[H-].[Li+].[Al+3].O.O.O.O.C(C(C(C([O-])=O)O)O)([O-])=O.[Na+].[K+].O.O(Cl)[Cl:46]>>[CH2:15]([N:12]1[CH:13]=[N:14][C:10]([CH2:8][NH:7][CH:1]2[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]2)=[N:11]1)[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1.[ClH:46]参加物
反応物 5
生成物 2
反応条件
- 温度
- 0 °C
実験手順
A solution of 1-benzyl-1H-[1,2,4]triazole-3-carboxylic acid cyclohexylamide (3.63 g, 12.8 mmol) in phosphosphorus oxychloride (10 mL) was heated at 70° C. for 4 hours. The solution was then concentrated. Toluene was added and then evaporated. The residue was dissolved in THF (100 mL). The solution was cooled to 0° C., and LiAlH4 (1.0 M in THF, 25.6 mL, 25.6 mmol) was added slowly into the solution. The solution was allowed to return to room temperature and then stirred for 1 hour. Potassium sodium tartrate tetrahydrate (5 g) was added. Water was added slowly to terminate the reaction. The solution was filtered and ethyl acetate was used to wash the filter cake. The filtrate was concentrated. HCl (1.0 M) in diethyl ether was added. The resulting precipitate was collected and recrystallized from acetone/methanol to yield (1-benzyl-1H-[1,2,4]triazol-3-ylmethyl)-cyclohexyl-amine as its corresponding hydrochloric acid salt, as a white solid.
後処理
- concentrationThe solution was then concentrated
- additionToluene was added
- customevaporated
- dissolutionThe residue was dissolved in THF (100 mL)
- customto return to room temperature
- customto terminate
- customthe reaction
- filtrationThe solution was filtered
- washto wash the filter cake
- concentrationThe filtrate was concentrated
- additionHCl (1.0 M) in diethyl ether was added
- customThe resulting precipitate was collected
- customrecrystallized from acetone/methanol
出典と根拠
- ORDレコード
- ord-420fc4034f9d46789a6038938521cdef
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07531545B2
反応ノート
読み込み中…