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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5379생성일: 2026년 10월 24일

1,1'-Carbonyldiimidazole → 4-Amino-N-(1-azabicyclo[3.3.1]non-5-ylmethyl)-5-chloro-2-(2-methoxyethoxy)benzamide

https://huagongshe.com/ko/reaction/5379

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참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물4-Amino-5-chloro-2-(2-methoxyethoxy)benzoic acidHCID 19795977—
반응물{1-Azabicyclo[3.3.1]nonan-5-yl}methanamineHCID 19795986—
용매TetrahydrofuranHCID 8028—
생성물4-Amino-N-(1-azabicyclo[3.3.1]non-5-ylmethyl)-5-chloro-2-(2-methoxyethoxy)benzamideHCID 1979598349%

반응 조건

온도0 °C

반응 단계

A solution of 4-amino-5-chloro-2-(2-methoxyethoxy)benzoic acid (2.09 g, 8.5 mmol) in anhydrous tetrahydrofuran (10 mL) under nitrogen was treated with 1,1'-carbonyldiimidazole (1.46 g, 9.0 mmol), stirred for one hour, degassed under a stream of nitrogen over 10 minutes, and cooled (0° C.). A solution of 1-azabicyclo[3.3.1]nonane-5-methanamine (1.36 g, 8.8 mmol) in tetrahydrofuran (5 mL) was added dropwise, and stirring was continued at room temperature for 18 hours. The solution was concentrated in vacuo and the residue was taken up in methylene chloride (100 mL) and washed with saturated sodium carbonate (50 mL). The organic solution was dried (Na2SO4), concentrated in vacuo, and passed through a short column of alumina (eluted with 5% methanol/methylene chloride). The filtrate was concentrated in vacuo and, at this point, appeared to be contaminated with some highly insoluble impurity. The residue was taken up in tetrahydrofuran and filtered, and the filtrate was concentrated in vacuo, triturated from cold ether, and recrystallized from acetonitrile (2 crops) to afford 1.59 g (49%) of colorless crystals; mp 154.0°-155.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244907
출처 데이터셋uspto-grants-1993_09
ORD IDord-27b03df9a5db4ae9b9cafbfe76f1aac5
출처 메모uspto-grants-1993_09