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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2217964생성일: 2026년 10월 26일

Ethyl 5-aminopyridazine-4-carboxylate → 5-[2-(2,4,6-Trifluorophenyl)-acetylamino]-pyridazine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2217964

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 5-aminopyridazine-4-carboxylateHCID 12352298—
반응물2,4,6-Trifluorophenylacetyl chlorideHCID 57428015—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매TolueneHCID 1140—
생성물5-[2-(2,4,6-Trifluorophenyl)-acetylamino]-pyridazine-4-carboxylic acid ethyl esterHCID 68939424101.7%

반응 조건

온도70 °C

반응 단계

5-Aminopyridazine-4-carboxylic acid ethyl ester (1.26 g, prepared according to J. Het. Chem., (1968), 5, 845) was dissolved in dry toluene (125 ml) at 90° C., and DMAP (0.92 g) was added. 2,4,6-Trifluorophenylacetyl chloride (1.75 g of 95% purity material) was added dropwise with stirring at 70° C., and a white solid precipitated. The reaction was stirred at reflux for 5 hours and then filtered hot. The filtrate was evaporated to give 5-[2-(2,4,6-trifluorophenyl)-acetylamino]-pyridazine-4-carboxylic acid ethyl ester as a white solid (2.6 g), m.p. 143-144° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07410967B2
출처 데이터셋uspto-grants-2008_08
ORD IDord-00ec7cec4a364349b01b9e1274154ad2
출처 메모uspto-grants-2008_08