반응 #161031
ord-4c76672ed7214cec939aabeedb7493a3
반응 방정식
반응 조건
후처리
- 1여과After the reaction solution was filtered
- 2농축the filtrate was concentrated under reduced pressure
- 3온도Under ice-cooling
- 4기타was returned to room temperature
- 5workup.STIRRINGwas stirred overnight
- 6기타The aqueous layer of the reaction solution was separately collected
- 7추출extracted with ethyl acetate
- 8세척after it was washed with a 10% potassium hydrogensulfate
- 9건조saturated brine, it was dried with anhydrous sodium sulfate
- 10workup.DISTILLATIONThe solvent was distilled off under reduced pressure and ether
- 11workup.ADDITIONwas added to the residue
- 12세척to wash the crystal
실험 절차
30 mg of 10% palladium-carbon was added to a solution of 350 mg (1 mmol) of N—[N-[(phenylmethoxy)carbonyl]-L-leucyl]-L-valinol obtained in Reference Example 184 in 10 ml of methanol, and the mixture was stirred under a hydrogen atmosphere at room temperature overnight. After the reaction solution was filtered, the filtrate was concentrated under reduced pressure. 10 ml of ethyl acetate, 10 ml of water and further 159 mg (1.5 mmol) of sodium carbonate were added to the residue. Under ice-cooling, a solution of 131 mg (1 mmol) of 2-furancarbonyl chloride in 3 ml of ethyl acetate was added to the mixture solution. The reaction solution was returned to room temperature and was stirred overnight. The aqueous layer of the reaction solution was separately collected and extracted with ethyl acetate. The organic layer was combined and after it was washed with a 10% potassium hydrogensulfate and then saturated brine, it was dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and ether was added to the residue to wash the crystal to obtain 268 mg (86%) of the title compound.