反応式
[C:1]([C:3]1[C:11]2[C:6](=[C:7]([C:12]([N:14]3[CH2:19][CH2:18][N:17]([CH2:20][CH2:21][C:22]4[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=4)[CH2:16][CH2:15]3)=[O:13])[CH:8]=[CH:9][CH:10]=2)[NH:5][CH:4]=1)#[N:2].[P:29](=[O:33])([OH:32])([OH:31])[OH:30]>CC(C)=O>[OH2:13].[P:29]([OH:33])([OH:32])([OH:31])=[O:30].[C:1]([C:3]1[C:11]2[C:6](=[C:7]([C:12]([N:14]3[CH2:15][CH2:16][N:17]([CH2:20][CH2:21][C:22]4[CH:23]=[CH:24][C:25]([F:28])=[CH:26][CH:27]=4)[CH2:18][CH2:19]3)=[O:13])[CH:8]=[CH:9][CH:10]=2)[NH:5][CH:4]=1)#[N:2]参加物
反応条件
- 温度
- 55 °C
実験手順
Add (3-cyano-1H-indol-7-yl)-[4-(4-fluorophenethyl)piperazin-1-yl]methanone (12.00 g 31.9 mmol) and acetone (300 mL) to a 500 mL flask equipped with overhead agitation, heating mantle, and condenser. Heat the slurry to about 55° C. to provide a homogeneous solution. Add a solution of concentrated (86% by weight) phosphoric acid (4.00 g, 35.1 mmol, 1.1 equiv) over 1 minute. The salt may begin to precipitate after approximately half of the phosphoric acid is added. After the addition is complete, heat the mixture to about 55° C. for 2 hours. Remove the heating mantle and allow the slurry to cool to about 22° C. and then stir for 2 hours. Filter the mixture and wash the filter cake twice with 30 mL acetone. Dry the solid for 20 hours in a vacuum oven at about 50° C. to provide 14.15 g (93% yield) of the title crystal form as a white solid. Initially, this process may produce a precipitate that may be gummy, but may become granular upon further stirring.
後処理
- customequipped with overhead agitation
- temperatureheating mantle
- customto provide a homogeneous solution
- additionAdd a solution
- customto precipitate after approximately half of the phosphoric acid
- additionis added
- additionAfter the addition
- temperatureheat the mixture to about 55° C. for 2 hours
- customRemove the heating mantle
- temperatureto cool to about 22° C.
- filtrationFilter the mixture
- washwash the filter cake twice with 30 mL acetone
- customDry the solid for 20 hours in a vacuum oven at about 50° C.
出典と根拠
- ORDレコード
- ord-cf0696b985c24bacaa7b919b79dd43f5
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08188087B2
関連ノート
読み込み中…