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HRID 1387678作成日:2026年10月27日

Omeprazole → 3-Chlorobenzoic Acid

https://huagongshe.com/reaction/1387678

反応式

関与物質

役割名称HCID仕込み量
反応物OmeprazoleHCID 4594—
反応物m-Chloroperbenzoic acidHCID 70297—
反応物TimoprazoleHCID 72171—
反応物2-((pyridin-2-ylmethyl)thio)-1H-benzo[d]imidazoleHCID 683949—
溶媒ChloroformHCID 6212—
生成物3-Chlorobenzoic AcidHCID 447—

反応条件

温度5 °C

反応手順

5-methoxy-2-[(4-methoxy-3,5-dimethyl-2-pyridyl)methyl]sulfinyl- 1H-benzimidazole (omeprazole) was disclosed for the first time in U.S. Pat. No. 4,255,431. In the process of preparing 2-(2-pyridylmethylsulfinyl)benzimidazole compounds there is mentioned an oxidation of corresponding 2-(2-pyridylmethylthio)benzimidazole compounds with 3-chloroperoxybenzoic acid in a chloroform solution under stirring and cooling at a temperature under 5° C. 3-chlorobenzoic acid formed is then filtered off, the filtrate is diluted with methylene chloride, washed with Na2CO3, dried with Na2SO4, evaporated in vacuo and the residue is crystallized under addition of CH3CN. Since omeprazole is unstable in an acidic medium, the cooling of the reaction mixture to 5° C. is necessary to prevent a decomposition of the omeprazole formed.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06268502B1
出典データセットuspto-grants-2001_07
ORD IDord-870ea6c530364bcab1c884964fa1820a
出典メモuspto-grants-2001_07