Hydrochloric Acid → HCID 178513764、化合物
反応式
[C:1]1([NH:7][C:8]2[C:12]([C:13]#[N:14])=[CH:11][N:10](COCC[Si](C)(C)C)[N:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1(NC2N(C[O:36]CC[Si](C)(C)C)N=CC=2C#N)C=CC=CC=1.Cl.C([O-])([O-])=O.[Na+].[Na+]>CCO.O>[C:1]1([NH:7][C:8]2[C:12]([C:13]([NH2:14])=[O:36])=[CH:11][NH:10][N:9]=2)[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 2
反応条件
- 温度
- 0 °C
実験手順
To a solution containing a mixture of 3-(phenylamino)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazole-4-carbonitrile and 5-(phenylamino)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazole-4-carbonitrile (2.6 g, 7.8 mmol) in EtOH (40.3 mL) was added 2N aqueous HCl (40.3 mL). The resulting mixture was heated at 0° C. for 1 hour. The mixture was cooled to ambient temperature and carefully neutralized with 3N aqueous Na2CO3 until pH ˜9. The solution was further diluted with H2O (400 mL), the layers were partitioned and the aqueous mixture was extracted with EtOAc (2×). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The crude residue was adsorbed on silica gel in vacuo and purified by MPLC on silica gel (using a gradient elution of 0-100% EtOAc/DCM) to afford the title compound, which was used without further purification.
後処理
- additionTo a solution containing
- temperatureThe mixture was cooled to ambient temperature
- customthe layers were partitioned
- extractionthe aqueous mixture was extracted with EtOAc (2×)
- washThe combined organic layers were washed with brine
- dry with materialdried over anhydrous Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- custompurified by MPLC on silica gel (
- washa gradient elution of 0-100% EtOAc/DCM)
出典と根拠
- ORDレコード
- ord-c992f5552cbd41a0921362693dd21240
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08962608B2
反応ノート
読み込み中…