戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 32042作成日:2026年10月25日

Methanol → HCID 178497006、化合物

https://huagongshe.com/reaction/32042

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物N-IodosuccinimideHCID 120273—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物HCID 178497005HCID 178497005—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178497006HCID 17849700669.3%

反応条件

温度0 °C

反応手順

7-Fluoro-6-o-tolylamino-1H-benzoimidazole-5-carboxylic acid methyl ester 7a (1.47 g, 4.92 mmol) is suspended in 1:1 THF:MeOH mixture (44 mL) and cooled to −78° C. under a nitrogen atmosphere. A solution of NIS (1.66 g, 7.39 mmol) in THF (2 mL) is added followed by a MeOH (2 mL) solution of TsOH—H2O (1.87 g, 9.84 mmol). After 30 minutes, the reaction mixture is warmed to 0° C. and 1 mL methylene chloride is added. The reaction is slowly allowed to warm to room temperature with stirring over 16 hours. The reaction mixture is quenched by the addition of 10% Na2S2O4 solution. The reaction mixture is then diluted with water and ethyl acetate and the layers separated. The aqueous layer is extracted with ethyl acetate. The combined organic extracts are dried (Na2SO4) and concentrated under reduced pressure. The recovered solid is triturated with MeOH to give 1.45 g (69%) pure desired product: MS ESI (+) m/z 426 (M+1) detected; MS ESI (−) m/z 424 (M−1) detected.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425637B2
出典データセットuspto-grants-2008_09
ORD IDord-5da8464ba7e44518a42beb98a1c95679
出典メモuspto-grants-2008_09