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HRID 602146作成日:2026年10月25日

Water → Methyl 2-[3-[[2-(4-chlorophenyl)-4-methylthiazol-5-yl]carbonylaminomethyl]pyrrolidin-1-yl]benzoate

https://huagongshe.com/reaction/602146

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物Benzoic acid, 2-fluoro-, methyl esterHCID 67854—
反応物N-(Pyrrolidin-3-yl methyl)-2-(4-chlorophenyl)-4-methylthiazole-5-carboxamideHCID 58992652—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒Dimethyl SulfoxideHCID 679—
生成物Methyl 2-[3-[[2-(4-chlorophenyl)-4-methylthiazol-5-yl]carbonylaminomethyl]pyrrolidin-1-yl]benzoateHCID 5899261558%

反応条件

温度140 °C

反応手順

N-(Pyrrolidin-3-yl methyl)-2-(4-chlorophenyl)-4-methylthiazole-5-carboxamide (168 mg, 0.500 mmol) and methyl 2-fluorobenzoate (0.127 mL, 1.00 mmol) were dissolved in dimethylsulfoxide (4 mL). To this solution, potassium carbonate (138 mg, 1.00 mmol) and tetrabutylammonium iodide (18.5 mg, 0.0500 mmol) were added and the mixture was stirred at 140° C. for 6 hours. Subsequently, the reaction mixture was allowed to cool and water was added. The mixture was then extracted with ethyl acetate and the extract washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=4:1->2:1) gave 136 mg (58%) of the desired compound as a colorless amorphous product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07902367B2
出典データセットuspto-grants-2011_03
ORD IDord-f569914275bf4e65bc69dfc738e7627e
出典メモuspto-grants-2011_03