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HRID 407068作成日:2026年10月26日

2-Butenenitrile → 1-[3-[7-[1-(1-Cyanopropan-2-yl)pyrazol-4-yl]imidazo[1,2-b]pyridazin-3-yl]phenyl]-3-(2,2,2-trifluoroethyl)urea

https://huagongshe.com/reaction/407068

反応式

関与物質

役割名称HCID仕込み量
反応物2-ButenenitrileHCID 20913—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物N-[3-(7-{-1H-pyrazol-4-yl}imidazo[1,2-b]pyridazin-3-yl)phenyl]-N'-(2,2,2-trifluoroethyl)ureaHCID 67980550—
溶媒MethanolHCID 887—
溶媒AcetonitrileHCID 6342—
生成物1-[3-[7-[1-(1-Cyanopropan-2-yl)pyrazol-4-yl]imidazo[1,2-b]pyridazin-3-yl]phenyl]-3-(2,2,2-trifluoroethyl)ureaHCID 57386677—

反応条件

温度60 °C

反応手順

To a solution of N-{3-[7-(1H-pyrazol-4-yl)imidazo[1,2-b]pyridazin-3-yl]phenyl}-N′-(2,2,2-trifluoroethyl)urea (15 mg, 0.037 mmol) and 2-butenenitrile (3.8 mg, 0.056 mmol) in acetonitrile (0.5 mL) and methanol (0.2 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (5.6 μL, 0.037 mmol). The mixture was stirred at 60° C. overnight. The reaction mixture was stirred at 60° C. overnight. The mixture was purified by RP-HPLC (pH=10) to afford the desired product. LCMS (M+H)+: m/z=469.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754114B2
出典データセットuspto-grants-2014_06
ORD IDord-6665bd91046d4d8494858e2ef5e05208
出典メモuspto-grants-2014_06