HCID 13935138、化合物 → 9-(((2-(Trifluoromethyl)phenyl)methyl)imino)-1,2,3,4,9,10-hexahydroacridin-1-ol
反応式
[F:1][C:2]([F:27])([F:26])[C:3]1[CH:25]=[CH:24][CH:23]=[CH:22][C:4]=1[CH2:5][NH:6][C:7]1[C:8]2[C:13]([N:14]=[C:15]3[C:20]=1[C:19](=[O:21])[CH2:18][CH2:17][CH2:16]3)=[CH:12][CH:11]=[CH:10][CH:9]=2.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[F:26][C:2]([F:1])([F:27])[C:3]1[CH:25]=[CH:24][CH:23]=[CH:22][C:4]=1[CH2:5][NH:6][C:7]1[C:8]2[C:13]([N:14]=[C:15]3[C:20]=1[CH:19]([OH:21])[CH2:18][CH2:17][CH2:16]3)=[CH:12][CH:11]=[CH:10][CH:9]=2参加物
4
反応条件
- 温度
- 10 °C
実験手順
In 100 ml of dry THF was dissolved 4.31 g of 3,4-dihydro-9-(2-trifluoromethylbenzylamino)acridin-1(2H)-one and the mechanically stirred solution was cooled to 10° C. under nitrogen. To it was added 5.8 ml of 1M LiAlH4 in THF dropwise over 15 minutes. Within 0.5 hours of addition the reaction was complete by TLC, so it was quenched with 1 ml of saturated ammonium chloride and the salts were filtered. The filtrate was evaporated to a solid which was dissolved in dichloromethane. The dichloromethane solution was dried over anhydrous magnesium sulfate and filtered. The filtrate was refluxed and pentane was added to effect crystallization. The crystals were collected from the cooled mother liquor to yield 3.44 g of solid, mp 158°-160° C.
後処理
- additionWithin 0.5 hours of addition the reaction
- customwas quenched with 1 ml of saturated ammonium chloride
- filtrationthe salts were filtered
- customThe filtrate was evaporated to a solid which
- dissolutionwas dissolved in dichloromethane
- dry with materialThe dichloromethane solution was dried over anhydrous magnesium sulfate
- filtrationfiltered
- temperatureThe filtrate was refluxed
- additionpentane was added to effect crystallization
- customThe crystals were collected from the cooled mother liquor
出典と根拠
- ORDレコード
- ord-bf9fd5460b42489e81efb25dd4ba0ad7
- 出典データセット
- uspto-grants-1988_06
- 特許番号
- US04754050
反応ノート
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