5-[3-(5-Cyano-1-ethyl-1,6-dihydro-4-methyl-2,6-dioxo-3(2H)-pyridinylidene)-1-propen-1-yl]-1-ethyl-1,2-dihydro-6-hydroxy-4-methyl-2-oxo-3-pyridinecarbonitrile → HCID 86757896, compound
Reaction equation
C([NH+:3](CC)CC)C.[C:8]([C:10]1[C:15](=[O:16])[N:14]([CH2:17][CH3:18])[C:13](=[O:19])[C:12](=[CH:20][CH:21]=[CH:22][C:23]2[C:24]([CH3:35])=[C:25]([C:33]#[N:34])[C:26](=[O:32])[N:27]([CH2:30][CH3:31])[C:28]=2[OH:29])[C:11]=1[CH3:36])#[N:9].C([O-])(=O)C.[NH4+]>C(O)(=O)C>[C:33]([C:25]1[C:26](=[O:32])[N:27]([CH2:30][CH3:31])[C:28](=[O:29])[C:23](=[CH:22][CH:21]=[CH:20][C:12]2[C:11]([CH3:36])=[C:10]([C:8]#[N:9])[C:15](=[O:16])[N:14]([CH2:17][CH3:18])[C:13]=2[OH:19])[C:24]=1[CH3:35])#[N:34].[NH4+:3]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
4.9 g of commercial triethylammonium 5-(3-(5-cyano-1-ethyl-4-methyl-2,6-dioxo-1,6-dihydro-2H -pyridin-3-ylidene)propenyl-1-ethyl-6-hydroxy-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile (24a) was made to react with 0.8 g of ammonium acetate in 75 mL of acetic acid as described under (a). This gave 3.6 g of dye (24a).
Sources & evidence
- ORD record
- ord-b7d91f0df61f4c0e8bf75f4751a6edba
- Source dataset
- uspto-grants-2002_03
- Patent number
- US06361571B1
Reaction notes
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