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HRID 5377作成日:2026年10月24日

1,1'-Carbonyldiimidazole → 4-Amino-N-(1-azabicyclo[3.2.1]oct-5-ylmethyl)-5-chloro-2-methoxybenzamide

https://huagongshe.com/ja/reaction/5377

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物4-Amino-5-chloro-2-methoxybenzoic acidHCID 81626—
反応物{1-Azabicyclo[3.2.1]octan-5-yl}methanamineHCID 19795979—
溶媒TetrahydrofuranHCID 8028—
生成物4-Amino-N-(1-azabicyclo[3.2.1]oct-5-ylmethyl)-5-chloro-2-methoxybenzamideHCID 1979597470%

反応手順

A suspension of 4-amino-5-chloro-2-methoxybenzoic acid (1.72 g, 8.5 mmol) in anhydrous tetrahydrofuan (10 mL) under nitrogen was treated with 1,1'-carbonyldiimidazole (1.46 g, 9.0 mmol), stirred for one hour, then degassed under a stream of nitrogen for 10 minutes. A solution of 1-azabicyclo[3.2.1]octane-5-methanamine (1.27 g, 9.0 mmol) in anhydrous tetrahydrofuran (8 mL) was added, and stirring was continued at room temperature for 18 hours and at 50° C. for one hour. The mixture was concentrated in vacuo and partitioned between toluene (100 mL) containing a little 2-propanol and saturated sodium carbonate (50 mL). The organic layer was separated and the organic solution was dried (Na2SO4), concentrated in vacuo, and triturated from cold ether. Recrystallization from acetonitrile (2 crops) afforded 1.92 g (70%) of colorless crystals; mp 185°-187° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244907
出典データセットuspto-grants-1993_09
ORD IDord-40169b770c9f42239cde7e0d4cb368b9
出典メモuspto-grants-1993_09