2,4-Hexadienoic Acid → HCID 20557509, compound
Reaction equation
[O:1]=[C:2]1[N:6]([CH2:7][CH2:8][C:9]([OH:11])=[O:10])[C:5](=[O:12])[NH:4][NH:3]1.[C:13]([OH:20])(=[O:19])[CH:14]=[CH:15][CH:16]=[CH:17][CH3:18]>C(#N)C>[C:13]([CH:14]1[CH:15]=[CH:16][CH:17]([CH3:18])[N:4]2[C:5](=[O:12])[N:6]([CH2:7][CH2:8][C:9]([OH:11])=[O:10])[C:2](=[O:1])[N:3]12)([OH:20])=[O:19]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a manner analogous to that described in Example 1(D), from 3,5-dioxo-1,2,4-triazolidine-4-propionic acid, prepared as described in Example 2(C) and hexa-2,4-dienoic acid, there was obtained in 76% yield 5-carboxy-2,3,5,8-tetrahydro-8-methyl-1,3-dioxo-1H-1,2,4-triazolo[1,2-a]pyridazine-2-propionic acid of melting point 184°-186° C. (from acetonitrile).
Workup
- customprepared
Sources & evidence
- ORD record
- ord-c56993df08784a1abdb09a31fe06d499
- Source dataset
- uspto-grants-1981_12
- Patent number
- US04307094
Reaction notes
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