HCID 23369594, compound → HCID 23369663, compound
Reaction equation
[CH2:1]([C:3]1[C:4](=[O:19])[NH:5][C:6]2[C:11]([CH:12]=1)=[C:10]([O:13]CC(C)=C)[CH:9]=[CH:8][C:7]=2[CH3:18])[CH3:2]>C(Cl)(Cl)Cl.CO.CCCCCC>[CH2:1]([C:3]1[C:4](=[O:19])[NH:5][C:6]2[C:11]([CH:12]=1)=[C:10]([OH:13])[C:9]([CH2:12][C:3]([CH3:4])=[CH2:1])=[CH:8][C:7]=2[CH3:18])[CH3:2]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Using 3-ethyl-5-(2-methyl-2-propenyl)oxy-8-methylcarbostyril (0.94 g, 3.66 mmol), the procedure of Reference Example 32 was followed (reaction, post-treatment, and recrystallization from chloroform-methanol-n-hexane) to obtain 710 mg of the title compound as pale yellow crystals (75.5%).
Sources & evidence
- ORD record
- ord-a2d7dabf41ac4b96a46ee2ca01b5ec45
- Source dataset
- uspto-grants-1996_11
- Patent number
- US05576324
Reaction notes
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