Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1070799생성일: 2026년 10월 25일
Methyl Acetate → N-{3-[4-amino-2-(ethoxymethyl)-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-1-yl]propyl}acetamide
https://huagongshe.com/reaction/1070799
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Methyl Acetate | HCID 6584 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Ammonium Hydroxide | HCID 14923 | — |
| 반응물 | Ammonium Acetate | HCID 517165 | — |
| 반응물 | tert-butyl 3-[2-(ethoxymethyl)-6,7-dimethyl-4-phenoxy-1H-imidazo[4,5-c]pyridin-1-yl]propylcarbamate | HCID 21973818 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | N-{3-[4-amino-2-(ethoxymethyl)-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-1-yl]propyl}acetamide | HCID 10236680 | — |
반응 단계
Ammonium acetate (500 g) and tert-butyl 3-[2-(ethoxymethyl)-6,7-dimethyl-4-phenoxy-1H-imidazo[4,5-c]pyridin-1-yl]propylcarbamate (35.09 g, 77 mmol) were combined in a 2 L flask. The neck of the flask was stuffed with a wad of paper towels. The reaction mixture was heated with stirring at 150° C. for 27 hours. The reaction mixture was allowed to cool to ambient temperature and then it was placed in an ice bath. Ammonium hydroxide was added until the pH reached 11. Sodium hydroxide (50%) was added until the pH reached 14. The resulting precipitate was isolated by filtration and then dissolved in chloroform (4 L). The chloroform solution was divided into two portions and each was washed with saturated potassium carbonate (2×2 L). The organics were combined, dried over magnesium sulfate and then concentrated under reduced pressure to provide 30.3 g of crude product. This material was slurried with methyl acetate to provide 13.7 g of N-{3-[4-amino-2-(ethoxymethyl)-6,7-dimethyl-1H-imidazo[4,5-c]pyridin 1-yl]propyl}acetamide as a gray solid, m.p. 161.8-162.3° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06903113B2 |
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| 출처 데이터셋 | uspto-grants-2005_06 |
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| ORD ID | ord-12b8961ab0ef4cd987102c58869964df |
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| 출처 메모 | uspto-grants-2005_06 |
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