반응식
[C:1]1([N:7]2[CH2:11][CH2:10][C:9](=O)[C:8]2=[O:13])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:14][N:15]1[CH2:19][CH2:18][CH2:17][CH:16]1[CH2:20][O:21][CH3:22].CCOCC>C1C=CC=CC=1>[CH3:22][O:21][CH2:20][CH:16]1[CH2:17][CH2:18][CH2:19][N:15]1[N:14]=[C:9]1[CH2:10][CH2:11][N:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[C:8]1=[O:13]참가 물질
5
실험 절차
A solution of the product of Example 61 and chiral 1-amino-2-methoxymethylpyrrolidine (SAMP or RAMP; 1 equiv) in benzene is refluxed under Dean-Stark conditions for 20 h After cooling, Et2O is added and the mixture is washed with water. The organic layer is dried (MgO4), and evaporated to give a residue which is chromatographed on silica gel to give the title compound.
후처리
- temperatureAfter cooling
- washthe mixture is washed with water
- customThe organic layer is dried (MgO4)
- customevaporated
- customto give a residue which
- customis chromatographed on silica gel
출처 및 근거
- ORD 기록
- ord-4025d25706be4a47bd53045e959c41ba
- 출처 데이터셋
- uspto-grants-1993_04
- 특허 번호
- US05202344
연결된 노트
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