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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 846611생성일: 2026년 10월 26일

1,1'-Carbonyldiimidazole → N-(3-Hydroxy-1-azabicyclo[2.2.2]oct-3-ylmethyl)-4-[(methylsulfonyl)amino]-benzamide hemihydrate

https://huagongshe.com/reaction/846611

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물4-(Methylsulfonamido)benzoic acidHCID 250653—
반응물3-(Aminomethyl)quinuclidin-3-olHCID 14789978—
용매TetrahydrofuranHCID 8028—
생성물N-(3-Hydroxy-1-azabicyclo[2.2.2]oct-3-ylmethyl)-4-[(methylsulfonyl)amino]-benzamide hemihydrateHCID 67894696105.9%

반응 단계

A solution/suspension of 4-[(methanesufonyl)amino]benzoic acid (1.62 g, 7.5 mmol) in anhydrous tetrahydrofuran (6 ml) under nitrogen was treated with 1,1'-carbonyldiimidazole (1.38 g, 8.5 mmol), stirred for 45 minutes, and degassed under a stream of nitrogen over 15 minutes. A solution of 3-hydroxy-1-azabicyclo[2.2.2]oct-3-ylmethanamine (1.56 g, 10 mmol) in anhydrous tetrahydrofuran (6 mL) was added, and the mixture soon became cloudy. After 18 hours at room temperature and 90 minutes at 50° C. the mixture was concentrated in vacuo and the residue was triturated from acetonitrile. The foamy solid thus obtained was filtered through alumina (eluted with 1:1 methanol/tetrahydrofuran) and the filtrate was concentrated in vacuo and recrystallized from 2-propanol/ether to afford 1.92 g (71%) of the title compound as a hygroscopic voluminous colorless solid (water soluble); mp 123°-125° C. (foam).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05137895
출처 데이터셋uspto-grants-1992_08
ORD IDord-ee0fd5ad773145a4b10a3650b6265a80
출처 메모uspto-grants-1992_08