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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5377생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물4-Amino-5-chloro-2-methoxybenzoic acidHCID 81626—
반응물{1-Azabicyclo[3.2.1]octan-5-yl}methanamineHCID 19795979—
용매TetrahydrofuranHCID 8028—
생성물4-Amino-N-(1-azabicyclo[3.2.1]oct-5-ylmethyl)-5-chloro-2-methoxybenzamideHCID 1979597470%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244907
출처 데이터셋uspto-grants-1993_09
ORD IDord-40169b770c9f42239cde7e0d4cb368b9
출처 메모uspto-grants-1993_09