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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | 4-(Methylsulfonamido)benzoic acid | HCID 250653 | — |
| 반응물 | 3-(Aminomethyl)quinuclidin-3-ol | HCID 14789978 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-(3-Hydroxy-1-azabicyclo[2.2.2]oct-3-ylmethyl)-4-[(methylsulfonyl)amino]-benzamide hemihydrate | HCID 67894696 | 105.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05137895 |
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| 출처 데이터셋 | uspto-grants-1992_08 |
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| ORD ID | ord-ee0fd5ad773145a4b10a3650b6265a80 |
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| 출처 메모 | uspto-grants-1992_08 |
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