氯化铵 → (Z)-5-[5-amino-2,3-dihydro-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2-oxo-1H-indol-4-yl]-4-pentynoic acid methyl ester
反应方程式
[CH3:1][O:2][C:3](=[O:29])[CH2:4][CH2:5][C:6]#[C:7][C:8]1[C:16]([N+:17]([O-])=O)=[CH:15][CH:14]=[C:13]2[C:9]=1/[C:10](=[CH:21]/[C:22]1[NH:23][CH:24]=[CH:25][C:26]=1[O:27][CH3:28])/[C:11](=[O:20])[NH:12]2.[Cl-].[NH4+]>O.CO.[Zn]>[CH3:1][O:2][C:3](=[O:29])[CH2:4][CH2:5][C:6]#[C:7][C:8]1[C:16]([NH2:17])=[CH:15][CH:14]=[C:13]2[C:9]=1/[C:10](=[CH:21]/[C:22]1[NH:23][CH:24]=[CH:25][C:26]=1[O:27][CH3:28])/[C:11](=[O:20])[NH:12]2参与物
6
反应物 2
产物 1
试剂、催化剂与溶剂 3
实验过程
Using Method L above, (Z)-5-[2,3-dihydro-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-5-nitro-2-oxo-1H-indol-4-yl]-4-pentynoic acid methyl ester (0.22 g, 0.57 mmol) (from Example 35 above) was reduced with zinc (0.33 g, 5.1 mmol) and ammonium chloride (67.1 mg, 1.25 mmol) in 10% water in methanol (20 mL) with heating at reflux for 4 h to give (Z)-5-[5-amino-2,3-dihydro-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2-oxo-1H-indol-4-yl]-4-pentynoic acid methyl ester (Yield 0.1 g, 48%).
后处理
- temperaturewith heating
- temperatureat reflux for 4 h
来源与证据
- ORD记录
- ord-a7497141d7a94c99a0004b2567ec4193
- 来源数据集
- uspto-grants-2001_06
- 专利号
- US06252086B1
反应笔记
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