4-{4-[(4,5-dichloro-1-ethyl-1H-indole-2-carbonyl)-amino]-phenyl}-piperazine-1-carboxylic acid tert-butyl ester → 4,5-Dichloro-1-ethyl-1h-indole-2-carboxylic acid (4-piperazin-1-yl-phenyl)-amide hydrochloride salt
反応式
C(OC([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[CH:19]=[CH:18][C:17]([NH:20][C:21]([C:23]3[N:24]([CH2:34][CH3:35])[C:25]4[C:30]([CH:31]=3)=[C:29]([Cl:32])[C:28]([Cl:33])=[CH:27][CH:26]=4)=[O:22])=[CH:16][CH:15]=2)[CH2:10][CH2:9]1)=O)(C)(C)C>C(Cl)Cl.Cl.O1CCOCC1>[ClH:32].[N:11]1([C:14]2[CH:19]=[CH:18][C:17]([NH:20][C:21]([C:23]3[N:24]([CH2:34][CH3:35])[C:25]4[C:30]([CH:31]=3)=[C:29]([Cl:32])[C:28]([Cl:33])=[CH:27][CH:26]=4)=[O:22])=[CH:16][CH:15]=2)[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1参加物
5
反応物 1
生成物 1
試薬・触媒・溶媒 3
実験手順
A mixture of 4-{4-[(4,5-dichloro-1-ethyl-1H-indole-2-carbonyl)-amino]-phenyl}-piperazine-1-carboxylic acid tert-butyl ester (750 mg, 1.45 mmol) in 15 mL of methylene chloride and 2 mL of 4M hydrogen chloride in dioxane was stirred at room temperature for 24 hr. The solvent was removed to afford 4,5-dichloro-1-ethyl-1H-indole-2-carboxylic acid (4-piperazin-1-yl-phenyl)-amide hydrochloride salt (700 mg, 99% yield) as an off white solid. LCMS for C21H22Cl2N4O calcd. (m/e) 416, observed 417 (M+H).
後処理
- customThe solvent was removed
出典と根拠
- ORDレコード
- ord-7f2ea9fa88c944269e0624e855b213dc
- 出典データセット
- uspto-grants-2012_02
- 特許番号
- US08124766B2
反応ノート
読み込み中…