반응 #45872
ord-86b2c1cb486d4551bdda45bf80d26985
반응 방정식
반응물
시약
반응 조건
후처리
- 1기타the solvent was evaporated away under reduced pressure
- 2workup.ADDITIONEther was added to the residue
- 3농축this was concentrated under reduced pressure
- 4workup.ADDITIONEther was added to the residue
- 5기타followed by sonication
- 6기타the solvent was removed with a pipette
- 7기타The residue was dried at 60° C. under reduced pressure for 2 hours
실험 절차
2-Cyclopropyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-6-(3-hydroxycyclopent-1-enyl)-5-methyl-1,3-benzoxazole-4-carbonitrile (I-306) (83 mg, 0.21 mmol) was dissolved in ethanol (0.85 ml) and diethyl ether (1.7 ml), and at room temperature, 1 M hydrochloric acid/ethanol solution (222 μl, 0.22 mmol) was added. After stirring at the same temperature for 4 hours, the solvent was evaporated away under reduced pressure. Ether was added to the residue, and this was concentrated under reduced pressure. This operation was repeated once again. Ether was added to the residue, followed by sonication, and the solvent was removed with a pipette. The residue was dried at 60° C. under reduced pressure for 2 hours to obtain the entitled compound (62 g, 65%) as a brown solid.