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HRID 70239作成日:2026年10月23日

Potassium Carbonate → methyl N-[[2-chloro-5-[1-(4-chlorophenyl)-1H-pyrazol-3-yl]phenyl]methyl]-carbamate

https://huagongshe.com/ja/reaction/70239

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1-Chloro-4-iodobenzeneHCID 12510—
反応物trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
反応物HCID 178502067HCID 178502067—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒1,4-DioxaneHCID 31275—
生成物methyl N-[[2-chloro-5-[1-(4-chlorophenyl)-1H-pyrazol-3-yl]phenyl]methyl]-carbamateHCID 66790277—

反応手順

To a mixture of methyl N-[[2-chloro-5-(1H-pyrazol-3-yl)phenyl]methyl]carbamate (i.e. the product of Step B, Example 4) (0.2 g, 0.75 mmol), trans-N,N′-dimethylcyclohexane-1,2-diamine (0.043 g, 0.3 mmol), copper(I) iodide (0.03 g, 0.15 mmol) and potassium carbonate (−325 mesh) (0.622 g, 4.5 mmol) in dioxane (4 mL) was added 1-chloro-4-iodobenzene (0.27 g, 1.13 mmol). The reaction mixture heated at reflux overnight and then concentrated under reduced pressure. The resulting residue was purified by medium pressure liquid chromatography (0 to 100% gradient of ethyl acetate in hexanes as eluant) to provide the title compound, a compound of the present invention, as a solid (0.156 g) melting at 151-153° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822521B2
出典データセットuspto-grants-2014_09
ORD IDord-c47034b563664e30a415a696704207da
出典メモuspto-grants-2014_09