Hydrochloric Acid → [4-(2-Methoxy-ethyl)-piperazin-1-yl]-benzoic acid hydrochloride
反応式
C[O:2][C:3](=[O:20])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[N:10]1[CH2:15][CH2:14][N:13]([CH2:16][CH2:17][O:18][CH3:19])[CH2:12][CH2:11]1.[ClH:21]>>[ClH:21].[CH3:19][O:18][CH2:17][CH2:16][N:13]1[CH2:14][CH2:15][N:10]([C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[C:3]([OH:20])=[O:2])[CH2:11][CH2:12]1参加物
3
実験手順
[4-(2-methoxy-ethyl)-piperazin-1-yl]-benzoic acid methyl ester (17 mmol) is dissolved in 4N HCl (70 ml) and heated under reflux for 5 hours. After cooling the solvent is evaporated and the residue is suspended in ethanol and the solid filtered of, washed with diethylether and dried (vacuum). A powder with mp. >270° C., Rf=0.35 (CH2Cl2/MeOH=9:1) is obtained.
後処理
- temperatureheated
- temperatureunder reflux for 5 hours
- temperatureAfter cooling the solvent
- customis evaporated
- filtrationthe solid filtered of,
- washwashed with diethylether
- customdried (vacuum)
- customA powder with mp. >270° C., Rf=0.35 (CH2Cl2/MeOH=9:1) is obtained
出典と根拠
- ORDレコード
- ord-e885f860ff0c4f559cf84f0bd45bf083
- 出典データセット
- uspto-grants-2003_11
- 特許番号
- US06642239B2
反応ノート
読み込み中…