반응식
[C:1]([O:5][C:6](=[O:27])[C:7]([O:10][C:11]1[CH:16]=[CH:15][C:14]([CH2:17][CH2:18][CH2:19][CH:20]2[C:24](=[O:25])[NH:23][C:22](=[O:26])[NH:21]2)=[CH:13][CH:12]=1)([CH3:9])[CH3:8])([CH3:4])([CH3:3])[CH3:2].[CH3:28][C:29]1[CH:30]=[C:31]([CH:34]=[CH:35][C:36]=1[CH3:37])[CH2:32]Cl.[O-]S([O-])(=O)=O.[Mg+2].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[C:1]([O:5][C:6](=[O:27])[C:7]([O:10][C:11]1[CH:16]=[CH:15][C:14]([CH2:17][CH2:18][CH2:19][CH:20]2[C:24](=[O:25])[N:23]([CH2:32][C:31]3[CH:34]=[CH:35][C:36]([CH3:37])=[C:29]([CH3:28])[CH:30]=3)[C:22](=[O:26])[NH:21]2)=[CH:13][CH:12]=1)([CH3:9])[CH3:8])([CH3:2])([CH3:3])[CH3:4]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
Compound 2-{4-[3-(2,5-dioxo-imidazolidin-4-yl)-propyl]-phenoxy}-2-methyl-propionic acid tert-butyl ester (0.29 g, 0.770 mmol) in DMF (10 mL) was treated with 3,4-dimethyl benzyl chloride (0.131 g, 0.847 mmol), MgSO4 (0.185 g, 1.54 mmol) and then 325 mesh K2CO3 (0.213 g, 1.54 mmol). The resultant mixture was heated to 50° C. under N2 for 4 h. The reaction mixture was cooled and quenched with 1N HCl (8 mL) and then extracted with EtOAc and water. The organic layer was dried (MgSO4) and the solvent was removed in vacuo to give a crude product which was purified by flash chromatography using a gradient of 4:1 then 1:1 hexanes:EtOAc to afford 0.202 g (53%) 2-(4-{3-[1-(3,4-dimethyl-benzyl)-2,5-dioxo-imidazolidin-4-yl]-propyl}-phenoxy)-2-methyl-propionic acid tert-butyl ester. MS (ES+) Calc'd for C29H39N2O5 (M+1) 495. Found m/z 495 (100%). 1H NMR.
후처리
- temperatureThe reaction mixture was cooled
- customquenched with 1N HCl (8 mL)
- extractionextracted with EtOAc and water
- dry with materialThe organic layer was dried (MgSO4)
- customthe solvent was removed in vacuo
- customto give a crude product which
- customwas purified by flash chromatography
출처 및 근거
- ORD 기록
- ord-734868c9c4e345aaa51151885a371aba
- 출처 데이터셋
- uspto-grants-2009_06
- 특허 번호
- US07544812B2
연결된 노트
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