Pyrrolidine → HCID 58277284, 화합물
반응식
[Cl:1][C:2]1[CH:3]=[C:4]([N:8]2[C:12]([C:13]3[CH:18]=[CH:17][CH:16]=[C:15]([O:19][CH2:20][CH2:21][CH2:22]Cl)[CH:14]=3)=[CH:11][C:10]([C:24]([O:26][CH2:27][CH3:28])=[O:25])=[N:9]2)[CH:5]=[CH:6][CH:7]=1.[NH:29]1[CH2:33][CH2:32][CH2:31][CH2:30]1>C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]([N:8]2[C:12]([C:13]3[CH:18]=[CH:17][CH:16]=[C:15]([O:19][CH2:20][CH2:21][CH2:22][N:29]4[CH2:33][CH2:32][CH2:31][CH2:30]4)[CH:14]=3)=[CH:11][C:10]([C:24]([O:26][CH2:27][CH3:28])=[O:25])=[N:9]2)[CH:5]=[CH:6][CH:7]=1참가 물질
4
실험 절차
41.5 mg (0.10 mmol) of the compound of Example 68A and 83 μl (0.99 mmol) of pyrrolidine in 3 ml of ethanol are stirred at 80° C. overnight. The reaction mixture is subsequently purified by preparative HPLC (RP18 column; mobile phase: acetonitrile/water gradient). 18.3 mg of the title compound are obtained.
후처리
- customThe reaction mixture is subsequently purified by preparative HPLC (RP18 column; mobile phase: acetonitrile/water gradient)
출처 및 근거
- ORD 기록
- ord-1f1135e03249432a89cb097bbd6b5596
- 출처 데이터셋
- uspto-grants-2013_03
- 특허 번호
- US08399682B2
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