反応 #51227
ord-7ceede82572049f485f3af7c071223a5
反応方程式
反応物
試薬
溶媒
反応条件
後処理
- 1温度cooling
- 2温度cooling for 1 hour
- 3抽出the mixture was extracted with ethyl acetate
- 4乾燥After the extract was dried over sodium sulfate
- 5その他the solvent was removed under reduced pressure
- 6workup.ADDITIONTo the residue were added 5 ml of dimethylformamide and 0.25 ml of morpholine
- 7workup.STIRRINGthe mixture was stirred at room temperature overnight
- 8workup.ADDITIONWater was added to the reaction mixture
- 9抽出the mixture was extracted with ethyl acetate
- 10乾燥After the extract was dried over anhydrous sodium sulfate
- 11その他the solvent was removed under reduced pressure
- 12その他The residue was purified by silica gel chromatography (solvent: chloroform-methanol=100:1)
- 13workup.ADDITIONThis compound was treated with palladium-carbon under hydrogen atmosphere
実験手順
0.15 ml of triethylamine and 0.07 ml of methanesulfonyl chloride were added to 10 ml of a tetrahydrofuranmethylene chloride suspension containing 0.31 g of N-benzyloxycarbonyl-trans-4-[(5-hydroxylmethyl-2-isoindolinyl)carbonyl]cyclohexylamine under ice-cooling, and the mixture was stirred under ice-cooling for 1 hour. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. After the extract was dried over sodium sulfate, the solvent was removed under reduced pressure. To the residue were added 5 ml of dimethylformamide and 0.25 ml of morpholine, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. After the extract was dried over anhydrous sodium sulfate, the solvent was removed under reduced pressure. The residue was purified by silica gel chromatography (solvent: chloroform-methanol=100:1). This compound was treated with palladium-carbon under hydrogen atmosphere to obtain trans-4-[(5-morpholinomethyl-2-isoindolinyl)carbonyl]cyclohexylamine (Reference Example 13-24 in Table 8).