HCID 46887808, compound → HCID 86735019, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:31]=[CH:32][C:33]=1[O:34][CH3:35])[CH2:6][O:7][C:8]([C:10]1C(C2C=CC=C([N+]([O-])=O)C=2)C(C(OC)=O)=C(C)[NH:14][C:15]=1[CH3:16])=[O:9]>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:31]=[CH:32][C:33]=1[O:34][CH3:35])[CH2:6][O:7][C:8](=[O:9])/[CH:10]=[C:15](\[NH2:14])/[CH3:16]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Analogously to Example 1 heating a solution of 75 mmols of 3'-n1trobenzylideneacetoacetic acid methyl ester and 75 mmols of β-aminocrotonic acid 3,4-dimethoxybenzyl ester in 120 ml of ethanol gave 2,6-dimethyl-3-methoxycarbonyl-4-(3'-nitrophenyl)-1,4-dihydropyridine-5-carboxylic acid 3,4-dimethoxybenzyl ester of melting point 129° C (from ethanol).
Sources & evidence
- ORD record
- ord-0add4589ab544cb5bf8806c1de2e747d
- Source dataset
- uspto-grants-1977_08
- Patent number
- US04044141
Reaction notes
Loading…