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HRID 2272680作成日:2026年10月25日

Phosgene → 1-(3-Tert-butyl-1-phenyl-1H-pyrazol-5-yl)-3-(2-fluoro-4-(1-N-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-7-yloxy)phenyl)urea

https://huagongshe.com/reaction/2272680

反応式

関与物質

役割名称HCID仕込み量
反応物PhosgeneHCID 6371—
反応物Sodium BicarbonateHCID 516892—
反応物3-tert-butyl-1-phenyl-1H-pyrazol-5-amineHCID 770634—
反応物7-(4-Amino-3-fluorophenoxy)-1-N-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-oneHCID 44184954—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3-Tert-butyl-1-phenyl-1H-pyrazol-5-yl)-3-(2-fluoro-4-(1-N-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-7-yloxy)phenyl)ureaHCID 53310623—

反応条件

温度0 °C

反応手順

3-Tert-butyl-1-phenyl-1H-pyrazol-5-amine (550 mg, 1.8 mmol) was dissolved in CH2Cl2 (25 mL) and an equal volume of saturated NaHCO3 (aq) was added. The biphasic mixture was stirred and cooled to 0° C. with an ice/water bath. After 10 minutes, 2 equiv. of a 1.9 M solution of phosgene in toluene were added. The mixture was vigorously stirred for 10 minutes, the organic layer was isolated, washed with H2O, dried (MgSO4) and concentrated to about 5 mL. This solution was added to a solution of the 7-(4-amino-3-fluorophenoxy)-1-N-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one (8a) (200 mg, 1.4 mmol) in THF. The solution was stirred for 15 hours at room temperature, the solvents were evaporated and the solid residue was washed with Et2O and CH2Cl2 to afford the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09120789B2
出典データセットuspto-grants-2015_09
ORD IDord-848e1e01051242feb60b23d1fe37ba52
出典メモuspto-grants-2015_09