تفاعل #87218

معادلة التفاعل

triethylamine

triethylamine

Oxalyl chloride

triethylamine

cyclohexanedione

6-Methyl-3-oxo-2-phenyl-2,3-dihydropyridazine-4-carboxylic acid

→

desired product

2-(6-Methyl-3-oxo-2-phenyl-2,3-dihydropyridazine-4-carbonyl)-cyclohexane-1,3-dione

المذيبات

dichloromethane

dichloromethane

ظروف التفاعل

المعالجة

1. 1
   تركيزAfter 1.5 h the reaction was concentrated in vacuo
2. 2
   أخرىThe residue obtained
3. 3
   أخرىproducing a reddish solution
4. 4
   أخرى(reaction monitored by LCMS)
5. 5
   workup.STIRRINGthe reaction was stirred overnight

الإجراء التجريبي

6-Methyl-3-oxo-2-phenyl-2,3-dihydropyridazine-4-carboxylic acid (0.56 g, 2.42 mmol) was stirred in anhydrous dichloromethane (13 ml) and 1 drop of anhydrous dimethylformamide was added. Oxalyl chloride (0.25 mL, 2.90 mmol) was added dropwise to the yellow solution. After 1.5 h the reaction was concentrated in vacuo. The residue obtained was dissolved in dichloromethane (20 ml). To the brown solution anhydrous triethylamine (1 ml), then cyclohexanedione (0.33 g, 2.90 mmol) was added, producing a reddish solution. A further 0.33 ml of anhydrous triethylamine was added. The reaction mixture was stirred at room temperature for 2 h (reaction monitored by LCMS), then acetone cyanohydrin (1 drop) and anhydrous triethylamine (0.67 ml) was added and the reaction was stirred overnight. LCMS indicated the desired product had been formed. The reaction mixture was concentrated in vacuo. The residue obtained was purified using column chromatography (SiO2, Toluene/Triethylamine/Dioxane/EtOH/Water 100:40:20:20:5 by volume) to afford the title compound as an orange oil (382 mg, 49%). 1H NMR (CDCl3) 2.05 (quin, 2H), 2.41 (m, 3H), 2.47 (br s, 2H), 2.73 (br s, 2H), 7.10 (s, 1H), 7.36 (m, 1H), 7.46 (m, 2H), 7.57 (m, 2H), 16.15 (br s, 1H) ppm.

المصدر