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HRID 40697作成日:2026年10月26日

Hydrochloric Acid → 3-[4-(4-Methanesulfonylpiperazin-1-yl)phenyl]-8-aza-bicyclo[3.2.1]octane

https://huagongshe.com/reaction/40697

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物1,4-DioxaneHCID 31275—
反応物3-[4-(4-Methanesulfonylpiperazin-1-yl)phenyl]-8-azabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl esterHCID 67412082—
溶媒DichloromethaneHCID 6344—
生成物3-[4-(4-Methanesulfonylpiperazin-1-yl)phenyl]-8-aza-bicyclo[3.2.1]octaneHCID 6741237086.3%

反応手順

3-[4-(4-Methanesulfonylpiperazin-1-yl)phenyl]-8-azabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester (0.758 g, 1.69 mmol) is solubilized in 158 ml of dichloromethane. 4N HCl in dioxane (4.2 ml, 16.8 mmol) is then added. After stirring for 16 h at ambient temperature, the reaction medium is concentrated, taken up with water, and washed with ethyl acetate. The pH of the aqueous phase is then adjusted to 10 with a 5N aqueous solution of sodium hydroxide. After extraction with dichloromethane, and washing with water and then with a saturated aqueous sodium chloride solution, the organic phase is dried over MgSO4 and then concentrated to dryness. 0.51 g of expected 3-[4-(4-methanesulfonylpiperazin-1-yl)phenyl]-8-aza-bicyclo[3.2.1]octane is obtained, which is subsequently used as it is.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530477B2
出典データセットuspto-grants-2013_09
ORD IDord-479e70835b7d462194d5dd9b232e2334
出典メモuspto-grants-2013_09