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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | 4-Amino-5-chloro-2-methoxybenzoic acid | HCID 81626 | — |
| 반응물 | {1-Azabicyclo[3.2.1]octan-5-yl}methanamine | HCID 19795979 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Amino-N-(1-azabicyclo[3.2.1]oct-5-ylmethyl)-5-chloro-2-methoxybenzamide | HCID 19795974 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05244907 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-40169b770c9f42239cde7e0d4cb368b9 |
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| 출처 메모 | uspto-grants-1993_09 |
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