反应方程式
[OH-].[Na+].[CH2:3]([C:5]1[CH:6]=[C:7]([C:12]([OH:14])=O)[S:8][C:9]=1[CH:10]=[O:11])[CH3:4].C([O:17][C:18](=[O:34])[CH2:19][CH2:20][C:21]1[C:26]([CH3:27])=[CH:25][C:24]([C:28](=[NH:31])[NH:29]O)=[CH:23][C:22]=1[CH2:32][CH3:33])C>CO>[CH2:32]([C:22]1[CH:23]=[C:24]([C:28]2[N:29]=[C:12]([C:7]3[S:8][C:9]([CH:10]=[O:11])=[C:5]([CH2:3][CH3:4])[CH:6]=3)[O:14][N:31]=2)[CH:25]=[C:26]([CH3:27])[C:21]=1[CH2:20][CH2:19][C:18]([OH:34])=[O:17])[CH3:33]参与物
5
反应物 3
产物 1
试剂、催化剂与溶剂 1
实验过程
The title compound is prepared according to Method E followed by treating the corresponding propionic ester derivative for 1 h at rt with 1 N aq. NaOH in methanol starting from 4-ethyl-5-formyl-thiophene-2-carboxylic acid and 3-[2-ethyl-4-(N-hydroxycarbamimidoyl)-6-methyl-phenyl]-propionic acid ethyl ester; LC-MS: tR=0.87 min; [M+1]+=399.20.
来源与证据
- ORD记录
- ord-f8f3008e3d9742c0bdfbcaf43f63633b
- 来源数据集
- uspto-grants-2012_04
- 专利号
- US08148410B2
关联笔记
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