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HRID1493312

反应详情

EQUATION

反应方程式

HRID 1493312 的结构方程式

REACTANTS

反应物

6
反应SMILES：O=CC=Cc1ccccc1
HCID307

3-Phenylprop-2-Enal

C9H8O

反应SMILES：C=CC(N)=O
HCID6579

Acrylamide

C3H5NO

反应SMILES：C=CC(=O)OCC
HCID8821

Ethyl acrylate

C5H8O2

反应SMILES：C=CC(=O)c1ccccc1
HCID13028

3-Oxo-3-phenylpropene

C9H8O

反应SMILES：O=C1C=CCCC1
HCID13594

2-Cyclohexen-1-one

C6H8O

反应SMILES：CCOC(=O)C1=C(C)NC(CS)=C(C(=O)OCC)C1c1cccc([N+](=O)[O-])c1
HCID11675833

未命名化合物

PRODUCTS

产物

1
反应SMILES：CCOC(=O)C1=CNC(C)=C(C(=O)OCC)C1c1cccc([N+](=O)[O-])c1
HCID9998606

未命名化合物

PROCEDURE

实验过程

Using in the procedure of Example 31 an α-β-unsatured-oxo compound selected from: cinnamaldehyde, ethyl acrylate, acrylamide, 1-phenyl-1-oxo-2-propene, 1-(p-imidazol-1-yl)phenyl-1-oxo-2-propene, 2-cyclohexen-1-one and 2-mercaptomethyl-3,5-dicarboethoxy-4-(m-nitrophenyl)-6-methyl-1,4-dihydropyridine, the following 3,5-dicarboethoxy-4-(m-nitrophenyl)-6-methyl-1,4-dihydropyridine are prepared: