반응 #51227
ord-7ceede82572049f485f3af7c071223a5
반응 방정식
반응물
시약
용매
반응 조건
후처리
- 1온도cooling
- 2온도cooling for 1 hour
- 3추출the mixture was extracted with ethyl acetate
- 4건조After the extract was dried over sodium sulfate
- 5기타the 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
- 9추출the mixture was extracted with ethyl acetate
- 10건조After the extract was dried over anhydrous sodium sulfate
- 11기타the solvent was removed under reduced pressure
- 12기타The residue was purified by silica gel chromatography (solvent: chloroform-methanol=100:1)
- 13workup.ADDITIONThis compound was treated with palladium-carbon under hydrogen atmosphere
실험 절차
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).