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HRID 383955作成日:2026年10月26日

P,P-Diphenylphosphinic azide → 1-Azabicyclo[3.2.1]oct-5-ylmethyl (5-phenyl-1,3-thiazol-4-yl)carbamate hydrochloride

https://huagongshe.com/reaction/383955

反応式

関与物質

役割名称HCID仕込み量
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物5-phenyl-1,3-thiazole-4-carboxylic AcidHCID 944813—
反応物{1-Azabicyclo[3.2.1]octan-5-yl}methanolHCID 19795992—
反応物1,4-Dioxane hydrochlorideHCID 20443148—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物1-Azabicyclo[3.2.1]oct-5-ylmethyl (5-phenyl-1,3-thiazol-4-yl)carbamate hydrochlorideHCID 86641070—

反応手順

To a solution of 5-phenyl-1,3-thiazole-4-carboxylic acid (400 mg) in toluene (5 mL) was added TEA (380 μL) at room temperature. To the reaction liquid was added dropwise a solution of DPPA (546 μL) in toluene (5 mL), followed by stirring at the same temperature for 20 minutes. After stirring at 90° C. for 5 minutes, a mixture of 1-azabicyclo [3.2.1]oct-5-yl methanol (357 mg) and DMF (2 mL) was added thereto, followed by heating under reflux for 1 hour. To the reaction liquid was added water, followed by extraction with EtOAc. The organic layer was washed with water and brine in this order, dried over MgSO4, and then concentrated under reduced pressure. The residue was purified by medium-pressure preparative liquid chromatography (YAMAZEN YFLC WPrep2XY, CHCl3:MeOH:28% aqueous ammonia=80:10:1) to obtain an oily substance. This was dissolved in EtOAc, followed by addition of 4 M HCl/dioxane at room temperature. The solid precipitated was collected by filtration and washed with EtOAc to obtain 1-azabicyclo[3.2.1]oct-5-ylmethyl (5-phenyl-1,3-thiazol-4-yl)carbamate hydrochloride (174 mg) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367696B2
出典データセットuspto-grants-2013_02
ORD IDord-c953148599a54aacbf477b9c834aa32d
出典メモuspto-grants-2013_02