HCID 68121768, compound → HCID 70593900, compound
Reaction equation
[F:1][C:2]([F:37])([F:36])[C:3]1[CH:35]=[CH:34][C:6]([CH2:7][O:8][C:9]([C:11]2C(C3C=CC=C([N+]([O-])=O)C=3)C(C(OC(C)C)=O)=C(C)[NH:15][C:16]=2[CH3:17])=[O:10])=[CH:5][CH:4]=1>C(O)C>[F:1][C:2]([F:36])([F:37])[C:3]1[CH:4]=[CH:5][C:6]([CH2:7][O:8][C:9](=[O:10])/[CH:11]=[C:16](\[NH2:15])/[CH3:17])=[CH:34][CH:35]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Analogously to Example 1 heating a solution of 75 mmols of 3'-nitrobenzylideneacetoacetic acid isopropyl ester and 75 mmols of β-aminocrotonic acid 4-trifluoromethylbenzyl ester in 120 ml of ethanol gave 2,6-dimethyl-3-isopropoxycarbonyl-4-(3'-nitrophenyl)-1,4-dihydropyridine-5-carboxylic acid 4-trifluoromethylbenzyl ester of melting point 139° C (from ethanol).
Sources & evidence
- ORD record
- ord-d5ef532e37914a828633271344322d4c
- Source dataset
- uspto-grants-1977_08
- Patent number
- US04044141
Reaction notes
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