反応式
[C:1]([O:5][C:6](=[O:25])[NH:7][CH2:8][C:9]1[CH:10]=[CH:11][C:12]2[CH:16]=[C:15]([C:17]3[CH:22]=[CH:21][N:20]=[C:19](Cl)[N:18]=3)[S:14][C:13]=2[CH:24]=1)([CH3:4])([CH3:3])[CH3:2].[NH2:26][CH2:27][CH2:28][CH2:29][N:30]1[CH2:35][CH2:34][N:33]([CH3:36])[CH2:32][CH2:31]1>O1CCOCC1>[C:1]([O:5][C:6](=[O:25])[NH:7][CH2:8][C:9]1[CH:10]=[CH:11][C:12]2[CH:16]=[C:15]([C:17]3[CH:22]=[CH:21][N:20]=[C:19]([NH:26][CH2:27][CH2:28][CH2:29][N:30]4[CH2:31][CH2:32][N:33]([CH3:36])[CH2:34][CH2:35]4)[N:18]=3)[S:14][C:13]=2[CH:24]=1)([CH3:4])([CH3:3])[CH3:2]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture of [2-(2-chloropyrimidin-4-yl)-benzo[b]thiophen-6-ylmethyl]-carbamic acid tert-butyl ester (1.47 g, 3.90 mmol) and 1-(3-aminopropyl)-4-methylpiperazine (1.36 g, 8.60 mmol) in dioxane (38 mL) is refluxed for 3 hours. The solvent is removed and the residue is subjected to chromatography on silica gel, eluting with 2.0 M NH3/MeOH in CHCl3 0-10%, to obtain the title compound (1.36 g, 70% yield). ES+(m/z) 497 [M+H].
後処理
- temperatureis refluxed for 3 hours
- customThe solvent is removed
- washeluting with 2.0 M NH3/MeOH in CHCl3 0-10%
出典と根拠
- ORDレコード
- ord-09c30005acbf4e2d84c146f67df2fb9b
- 出典データセット
- uspto-grants-2009_06
- 特許番号
- US07547691B2
関連ノート
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