反応式
O.[OH-].[Li+].C[O:5][C:6]([C:8]1[CH:17]=[C:16]2[C:11]([C:12]([C:18]3[C:22]([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][N:24]=4)=[N:21][N:20]4[CH2:29][CH2:30][CH2:31][C:19]=34)=[CH:13][CH:14]=[N:15]2)=[CH:10][CH:9]=1)=[O:7]>O1CCCC1.O>[N:24]1[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=1[C:22]1[C:18]([C:12]2[C:11]3[C:16](=[CH:17][C:8]([C:6]([OH:7])=[O:5])=[CH:9][CH:10]=3)[N:15]=[CH:14][CH:13]=2)=[C:19]2[CH2:31][CH2:30][CH2:29][N:20]2[N:21]=1参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
Lithium hydroxide monohydrate (0.65 g, 15.6 mmol) is added to a solution of 4-(2-pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinoline-7-carboxylic acid methyl ester (1.44 g, 3.89 mmol) in 2:1 tetrahydrofuran/water (30 mL), stirred at room temperature for 18 h, and concentrated in vacuo. The residue is purified by SCX resin, (2 N ammonia in methanol), to yield the title compound, 1.22 g (88%), as a tan solid.
後処理
- concentrationconcentrated in vacuo
- customThe residue is purified by SCX resin, (2 N ammonia in methanol),
出典と根拠
- ORDレコード
- ord-482e9e53739947068ed5441ee039ebd0
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07087626B2
関連ノート
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