反応式
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([OH:24])=[C:6]([C@@H:8]([C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH2:9][CH2:10][N:11]([CH:15]([CH3:17])[CH3:16])[CH:12]([CH3:14])[CH3:13])[CH:7]=1.[NH:25]1[C:29](=[O:30])[CH2:28][CH2:27][C@H:26]1[C:31]([OH:33])=[O:32]>CC(C)=O>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([OH:24])=[C:6]([C@@H:8]([C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH2:9][CH2:10][N:11]([CH:12]([CH3:14])[CH3:13])[CH:15]([CH3:16])[CH3:17])[CH:7]=1.[NH:25]1[C:29](=[O:30])[CH2:28][CH2:27][C@H:26]1[C:31]([O-:33])=[O:32]参加物
4
実験手順
3.25 g of tolterodine dissolved in 50 mL of acetone was mixed at room temperature (25° C.) with 1.29 g of L-pyroglutamic acid, which was suspended in 50 mL of acetone, and then stirred. In 10 minutes, there started to appear a solid precipitate. 50 mL of acetone was added thereto and the mixture was stirred at room temperature (25° C.) for 1 hour. The resulting solid precipitate was filtered and then washed with acetone. The resultant was dried at room temperature (25° C.) for 24 hours and 3.74 g (theoretical yield: 82.3%) of the final product in white solid was obtained.
後処理
- stirringthe mixture was stirred at room temperature (25° C.) for 1 hour
- filtrationThe resulting solid precipitate was filtered
- washwashed with acetone
- customThe resultant was dried at room temperature (25° C.) for 24 hours
出典と根拠
- ORDレコード
- ord-61d10679dfec4d6bb30c69427de548b8
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08367726B2
関連ノート
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