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HRID 1354607作成日:2026年10月23日

1,4-Dioxane hydrochloride → 2-(4-Chloro-2-oxo-1,2-dihydro-pyridin-3-yl)-7-methyl-3H-benzimidazole-5-carbonitrile

https://huagongshe.com/ja/reaction/1354607

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Dioxane hydrochlorideHCID 20443148—
反応物2-(4-Iodo-2-methoxy-pyridin-3-yl)-7-methyl-3H-benzimidazole-5-carbonitrileHCID 22021013—
生成物2-(4-Chloro-2-oxo-1,2-dihydro-pyridin-3-yl)-7-methyl-3H-benzimidazole-5-carbonitrileHCID 135681642—

反応条件

温度80 °C

反応手順

A suspension of 2-(4-iodo-2-methoxy-pyridin-3-yl)-7-methyl-3H-benzimidazole-5-carbonitrile (1.8 g, 4.63 mmol) in 4 M HCl dioxane (40 mL) was heated to 80° C. for 6 h and cooled to room temperature. The precipitate was filtered and dried. The crude product (1.08 g, 82%) was used for the next step without purification. LRMS (neg. ESI, (M−H)−) m/z 283.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07223757B2
出典データセットuspto-grants-2007_05
ORD IDord-1e4f7bb0be984132832467b73edb6a6c
出典メモuspto-grants-2007_05