戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1296351作成日:2026年10月25日

Methanamine, N-methoxy-, hydrochloride (1:1) → N-Methoxy-N-methyl-5-(4-chlorophenyl)-1-(2-chlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/1296351

反応式

関与物質

役割名称HCID仕込み量
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
反応物Ethyl 1-(2-chlorophenyl)-5-(4-chlorophenyl)-4-methyl-1h-pyrazole-3-carboxylateHCID 58760952—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
生成物N-Methoxy-N-methyl-5-(4-chlorophenyl)-1-(2-chlorophenyl)-4-methyl-1H-pyrazole-3-carboxamideHCID 86592991—

反応条件

温度-25 °C

反応手順

Isopropylmagnesium chloride (15 ml, 30 mmol) was added dropwise over a 10 to 15 minute period to a stirred solution of ethyl 5-(4-chlorophenyl)-1-(2-chlorophenyl)-4-methyl-1H-pyrazole-3-carboxylate (8.15 g, 21.7 mmol) and N,O-dimethylhydroxylamine hydrochloride (1.51 g, 15.5 mmol) in THF at −25° C. After stirring for an additional 15 minutes at −25° C., the reaction mixture was quenched with saturated aqueous NH4Cl and then extracted with methyl-tert-butyl ether. The organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo to give the title compound I-1a as a golden oil (8.76 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07247628B2
出典データセットuspto-grants-2007_07
ORD IDord-d5e959fcaacf46199ae8e563b0a306ab
出典メモuspto-grants-2007_07