Sodium Hydroxide → HCID 18326251、化合物
反応式
[Cl:1][C:2]1[C:7]([C:8]([O:10]CC)=[O:9])=[CH:6][C:5]([C:13]2[C:17]([CH3:18])=[C:16]([C:19]#[N:20])[N:15]([CH3:21])[N:14]=2)=[C:4]([F:22])[CH:3]=1.[OH-].[Na+]>O1CCOCC1>[Cl:1][C:2]1[C:7]([C:8]([OH:10])=[O:9])=[CH:6][C:5]([C:13]2[C:17]([CH3:18])=[C:16]([C:19]#[N:20])[N:15]([CH3:21])[N:14]=2)=[C:4]([F:22])[CH:3]=1参加物
4
実験手順
3.1 g of 3-(4-chloro-2-fluoro-5-carbethoxyphenyl)-4-methyl-5-cyano-1-methyl-[1H]-pyrazole (Example H13) are dissolved in 22 ml of dioxane, and 10 ml of 2N aqueous sodium hydroxide solution are added dropwise at 22° C. The mixture is stirred until the reaction is complete, the solvent is evaporated, the resulting residue is dissolved in water and the solution is brought to pH 1using hydrochloric acid. The precipitate formed is filtered off and dried. This gives the desired product in a yield of 2.63 g (89.8% of theory).