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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11363생성일: 2026년 10월 26일

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/11363

반응식

참여 물질

역할이름HCID투입량
반응물Methyl AcetateHCID 6584—
반응물Sodium HydroxideHCID 14798—
반응물Ammonium HydroxideHCID 14923—
반응물Ammonium AcetateHCID 517165—
반응물tert-butyl 3-[2-(ethoxymethyl)-6,7-dimethyl-4-phenoxy-1H-imidazo[4,5-c]pyridin-1-yl]propylcarbamateHCID 21973818—
용매ChloroformHCID 6212—
생성물N-{3-[4-amino-2-(ethoxymethyl)-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-1-yl]propyl}acetamideHCID 10236680—

반응 조건

온도150 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098221B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-bb8d62be3b474153a939fe55c76cbba5
출처 메모uspto-grants-2006_08