반응식
[CH:1]1N=C[N:3]([C:6]([N:8]2C=N[CH:10]=[CH:9]2)=[O:7])[CH:2]=1.[CH3:13][O:14][C:15]1[CH:16]=C([CH:20]=[C:21]([O:25][CH3:26])[C:22]=1[O:23][CH3:24])CN.NC1[CH:36]=[CH:35][C:31]([C:32]([OH:34])=[O:33])=[CH:30][CH:29]=1>[OH-].[Na+]>[CH3:26][O:25][C:21]1[CH:20]=[C:10]([CH:16]=[C:15]([O:14][CH3:13])[C:22]=1[O:23][CH3:24])[CH2:9][NH:8][C:6](=[O:7])[NH:3][CH2:2][C:1]1[CH:36]=[CH:35][C:31]([C:32]([OH:34])=[O:33])=[CH:30][CH:29]=1참가 물질
5
실험 절차
N,N-carbonyldiimidazole (1.62 g, 10 mmol), 3,4,5-trimethoxybenzyl amine (1.97 g, 10 mmol), p-aminobenzoic acid (1.52 g, 10 mmol), and 10 ml of 1 mol/L sodium hydroxide are used according to the method for the production of compound III in Method two to obtain 3.54 g of 4-[(3,4,5-trimethoxybenzylureido)methyl]benzoic acid (intermediate M-35) as a white solid, with a yield of 94.6%.
출처 및 근거
- ORD 기록
- ord-3d01f9b77e7e44969a51c2bde6985c6f
- 출처 데이터셋
- uspto-grants-2014_11
- 특허 번호
- US08889876B2
연결된 노트
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