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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 522697생성일: 2026년 10월 24일

Acetic Acid → Methyl 2-(4-(pyridin-3-yl)benzylamino)thiazole-5-carboxylate

https://huagongshe.com/ko/reaction/522697

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Methyl 2-aminothiazole-5-carboxylateHCID 238005—
반응물4-(Pyridin-3-yl)benzaldehydeHCID 3693046—
반응물Sodium borohydrideHCID 4311764—
용매TolueneHCID 1140—
생성물Methyl 2-(4-(pyridin-3-yl)benzylamino)thiazole-5-carboxylateHCID 86665086—

반응 단계

To a 250 mL round-bottomed flask was added 4-(pyridin-3-yl)benzaldehyde (4 g, 21.8 mmol), methyl 2-aminothiazole-5-carboxylate (3.45 g, 21.83 mmol) and acetic acid (0.375 ml, 6.55 mmol) in toluene (109 ml). The reaction mixture was heated at reflux under Dean-Stark conditions for 3 hours, cooled to room temperature, and the volatiles were removed by rotary evaporation. Methanol was added, the solution was cooled to 0° C., and sodium borohydride (1.322 g, 34.9 mmol) was carefully added. The reaction was stirred at 0° C. for 15 minutes and allowed to warm to room temperature while stirring for an additional 2 hour. The solids were filtered off, washed with water and dried under high vacuum to give the title compound which was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09334264B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-c66c9fb567dc416e8910a24320d80ad9
출처 메모uspto-grants-2016_05