Reaction equation
CO[C:3](=[O:24])[C:4]([C:14](=[O:23])[C:15]1[CH:20]=[CH:19][C:18]([CH3:21])=[C:17]([CH3:22])[CH:16]=1)=[CH:5][NH:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([CH3:13])[N:8]=1>C1(OC2C=CC=CC=2)C=CC=CC=1>[CH3:22][C:17]1[CH:16]=[C:15]([CH:20]=[CH:19][C:18]=1[CH3:21])[C:14]([C:4]1[C:3](=[O:24])[C:12]2[C:7](=[N:8][C:9]([CH3:13])=[CH:10][CH:11]=2)[NH:6][CH:5]=1)=[O:23]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Experimental conditions analogous to those described for Step 2 of Example 1 were used with 0.59 g (1.82 mmol) of 2-(3,4-Dimethyl-benzoyl)-3-(6-methyl-pyridin-2-ylamino)-acrylic acid methyl ester in 30 mL of diphenyl ether to yield 0.33 g of 3-(3,4-Dimethyl-benzoyl)-7-methyl-1H-[1,8]naphthyridin-4-one as a brown solid.
Sources & evidence
- ORD record
- ord-9d3b8fdd93c247c9b0a0ecd481dbd9bb
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07557213B2
Linked notes
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