반응식
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[C:8]([C:19](O)=[O:20])[CH:9]=[C:10]([C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=2)[CH:11]=1)=[O:5])[CH3:2].Cl.CN(C)CCCN=C=NCC.O.ON1C2C=CC=CC=2N=N1.[CH3:45][C:46]1[N:51]=[CH:50][C:49]([CH2:52][NH2:53])=[CH:48][N:47]=1.C(N(CC)C(C)C)(C)C>C([O-])(O)=O.[Na+].CCOC(C)=O.C(Cl)Cl>[CH3:18][C:15]1[CH:16]=[CH:17][C:12]([C:10]2[CH:9]=[C:8]([C:19](=[O:20])[NH:53][CH2:52][C:49]3[CH:48]=[N:47][C:46]([CH3:45])=[N:51][CH:50]=3)[CH:7]=[C:6]([C:4]([O:3][CH2:1][CH3:2])=[O:5])[CH:11]=2)=[CH:13][CH:14]=1참가 물질
9
반응물 5
생성물 1
시약·촉매·용매 3
실험 절차
To a mixture of crude 5-(ethoxycarbonyl)-4′-methylbiphenyl-3-carboxylic acid (450 mg, 1.6 mmol), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (610 mg, 3.2 mmol), 1-hydroxybenzotriazole hydrate (240 mg, 1.6 mmol), CH2Cl2 (5 mL) were added (2-methylpyrimidin-5-yl)methanamine (290 mg, 2.4 mmol) and N,N-diisopropylethylamine (0.41 mL, 2.4 mmol). The reaction mixture was stirred at room temperature overnight, and then diluted with aq. NaHCO3 solution and EtOAc (100 mL). The organic layer was separated, washed with brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel column (0-20% MeOH/CH2Cl2) to afford the title product as a white foam.
후처리
- customThe organic layer was separated
- washwashed with brine
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated in vacuo
- customThe residue was purified by silica gel column (0-20% MeOH/CH2Cl2)
출처 및 근거
- ORD 기록
- ord-97d7561a4eaa4f94bb3082982c572994
- 출처 데이터셋
- uspto-grants-2015_02
- 특허 번호
- US08946439B2
연결된 노트
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