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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5378생성일: 2026년 10월 24일

1,1'-Carbonyldiimidazole → N-(1-Azabicyclo[3.3.1]non-5-ylmethyl)-5-chloro-2-methoxy-4-(methylamino)benzamide

https://huagongshe.com/ko/reaction/5378

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참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물5-Chloro-2-methoxy-4-(methylamino)benzoic acidHCID 11694216—
반응물{1-Azabicyclo[3.3.1]nonan-5-yl}methanamineHCID 19795986—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물N-(1-Azabicyclo[3.3.1]non-5-ylmethyl)-5-chloro-2-methoxy-4-(methylamino)benzamideHCID 1979597573.3%

반응 조건

온도0 °C

반응 단계

A solution of 5-chloro-2-methoxy-4-(methylamino)benzoic acid (1.08 g, 5 mmol) in anhydrous tetrahydrofuran (7 mL) under nitrogen was treated with 1,1'-carbonyldiimidazole (0.90 g, 5.5 mmol), stirred one hour, degassed under a stream of nitrogen for 10 minutes, and cooled (0° C.). A solution of 1-azabicyclo[3.3.1]nonane-5-methanamine (0.82 g, 5.3 mmol) in tetrahydrofuran (3 mL) was added dropwise, and stirring was continued at room temperature for 18 hours. The suspension was diluted with enough methanol to dissolve the solid, then the solution was filtered through a short column of alumina (eluted with 20% methanol/tetrahydrofuran). The filtrate was concentrated in vacuo, triturated from cold ether, and recrystallized from acetonitrile to afford 1.29 g (73%) of colorless crystals; mp 188°-190° C. (second phase), first phase melting point 175° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244907
출처 데이터셋uspto-grants-1993_09
ORD IDord-2a7ae11fb7f447428407b154948c0592
출처 메모uspto-grants-1993_09