Water → [2-(4-di-n-propylamino-butyl)-1,3-dioxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-carbamic acid t-butyl ester
반응식
[C:1]([O:5][C:6]([NH:8][CH2:9][C:10]1[CH:11]=[C:12]([C:19]([OH:21])=O)[C:13](=[CH:17][CH:18]=1)[C:14]([OH:16])=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:22]([N:25]([CH2:31][CH2:32][CH3:33])[CH2:26][CH2:27][CH2:28][CH2:29][NH2:30])[CH2:23][CH3:24].O>C1(C)C(C)=CC=CC=1>[C:1]([O:5][C:6](=[O:7])[NH:8][CH2:9][C:10]1[CH:11]=[C:12]2[C:13](=[CH:17][CH:18]=1)[C:14](=[O:16])[N:30]([CH2:29][CH2:28][CH2:27][CH2:26][N:25]([CH2:31][CH2:32][CH3:33])[CH2:22][CH2:23][CH3:24])[C:19]2=[O:21])([CH3:2])([CH3:3])[CH3:4]참가 물질
5
실험 절차
The compound (123 mg) obtained in Example 7-4 was dissolved in xylene (5.0 ml). A xylene solution (5.0 ml) containing the compound (83.4 mg) obtained in Example 1-2 was dropped to the solution and the whole was refluxed under heating for 63 hours. The solution was added with water to stop the reaction and then subjected to extraction with chloroform. The organic layer was washed with water and a saturated saline solution, followed by drying with anhydrous sodium sulfate. The residue obtained by distilling the solvent off was then purified through silica gel column chromatography (hexane/ethyl acetate), thereby obtaining the subject compound (88.4 mg) as a yellow solid.
후처리
- additionwas dropped to the solution
- temperaturethe whole was refluxed
- temperatureunder heating for 63 hours
- customthe reaction
- extractionsubjected to extraction with chloroform
- washThe organic layer was washed with water
- dry with materialby drying with anhydrous sodium sulfate
- customThe residue obtained
- distillationby distilling the solvent
- customoff was then purified through silica gel column chromatography (hexane/ethyl acetate)
출처 및 근거
- ORD 기록
- ord-53ac96361f5b40e3874e407376766ce2
- 출처 데이터셋
- uspto-grants-2011_04
- 특허 번호
- US07932281B2
반응 노트
불러오는 중…