反応式
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([C:12]3[C:16]([C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][N:18]=4)=[N:15][N:14]4[CH2:23][CH2:24][CH:25]([OH:26])[C:13]=34)=[CH:7][CH:8]=[N:9]2)=[CH:4][CH:3]=1.CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O>ClCCl>[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([C:12]3[C:16]([C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][N:18]=4)=[N:15][N:14]4[CH2:23][CH2:24][C:25](=[O:26])[C:13]=34)=[CH:7][CH:8]=[N:9]2)=[CH:4][CH:3]=1参加物
4
実験手順
To a solution of 3-(7-bromo-quinolin-4-yl)-2-pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-4-ol (89.0 mg, 0.22 mmol) in dry dichloromethane (2 mL) is added Dess-Martin periodinane (301.0 mg, 0.71 mmol) and the resulting mixture stirred for 18 h. The reaction mixture is chromatographed on SiO2 (dichloromethane to 20% methanol in dichloromethane) to yield a yellow solid, 78 mg (88%).
後処理
- customThe reaction mixture is chromatographed on SiO2 (dichloromethane to 20% methanol in dichloromethane)
- customto yield a yellow solid, 78 mg (88%)
出典と根拠
- ORDレコード
- ord-43ca1bcbc16d469a97431b90b39c825b
- 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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