Ammonia → 9-[(Cyclohexyl)methyl]-4-hydroxy-5-carbamoyl carbazole
反応式
[CH:1]1([CH2:7][N:8]2[C:20]3[CH:19]=[CH:18][CH:17]=[C:16]([OH:21])[C:15]=3[C:14]3[C:9]2=[CH:10][CH:11]=[CH:12][C:13]=3[C:22]([O:24]C)=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[NH3:26]>C1COCC1.[OH-].[NH4+]>[CH:1]1([CH2:7][N:8]2[C:20]3[CH:19]=[CH:18][CH:17]=[C:16]([OH:21])[C:15]=3[C:14]3[C:9]2=[CH:10][CH:11]=[CH:12][C:13]=3[C:22](=[O:24])[NH2:26])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1参加物
反応条件
- 温度
- 35 °C
実験手順
A solution of 9-[(cyclohexyl)methyl]-4-hydroxy-5-carbomethoxy carbazole (205 mg, 0.608 mmol) in 5 mL of THF and 20 mL of concentrated aqueous ammonium hydroxide was treated with a stream of NH3 gas to ensure saturation. The reaction vessel was capped, and the mixture was heated at 35° C. with stirring until tlc indicated complete consumption of starting material (20 hrs). The THF was evaporated, and the aqueous layer was filtered. The green solid precipitate was dissolved in THF and purified by radial chromatography on silica gel (elution with CH2Cl2). The resultant foam was triturated with ether to afford 138 mg (70%) of the title compound as an off-white solid. IR (KBr, cm−1) 3418, 3200, 3131, 1629, 1600, 1443, 1261, 778. 'FAB HRMS m/e, Calcd for C20H23N2O2: 323.1760. Found: 323.1760 (M+1).
後処理
- customThe reaction vessel was capped
- customconsumption of starting material (20 hrs)
- customThe THF was evaporated
- filtrationthe aqueous layer was filtered
- dissolutionThe green solid precipitate was dissolved in THF
- custompurified by radial chromatography on silica gel (elution with CH2Cl2)
- customThe resultant foam was triturated with ether
出典と根拠
- ORDレコード
- ord-f5d528bab89d4d118d3d4fdc70b1fc6d
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06713645B1
反応ノート
読み込み中…