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HRID 388083作成日:2026年10月26日

Potassium Carbonate → 1-(4-Methoxybenzyl)-6-(quinolin-5-YL)-1H-imidazo[4,5-B]pyrazin-2(3H)-one

https://huagongshe.com/reaction/388083

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Quinolin-5-ylboronic acidHCID 5153389—
反応物6-Bromo-N2-(4-methoxybenzyl)pyrazine-2,3-diamineHCID 24820429—
反応物(3-Amino-6-(5-quinolyl)pyrazin-2-yl)[(4-methoxyphenyl)methyl]amineHCID 66699817—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1-(4-Methoxybenzyl)-6-(quinolin-5-YL)-1H-imidazo[4,5-B]pyrazin-2(3H)-oneHCID 6669962415%

反応手順

(3-Amino-6-(5-quinolyl)pyrazin-2-yl)[(4-methoxyphenyl)methyl]amine. 6-Bromo-N2-(4-methoxybenzyl)pyrazine-2,3-diamine (0.928 g, 3.00 mmol), quinoline-5-boronic acid (0.675 g, 3.9 mmol), tetrakis(triphenylphosphine)palladium (0.306 g, 0.265 mmol), potassium carbonate (1.10 g, 7.95 mmol), water (7 ml) and dimethylformamide (35 mL) were reacted according to General Procedure B. The crude material was purified via Biotage silica gel chromatography (0-10% methanol in dichloromethane) followed by triturating with water/methanol to afford the title compound (0.165 g, 15% yield). MS (ESI) m/z 358.3 [M+1]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08372976B2
出典データセットuspto-grants-2013_02
ORD IDord-fb8e230fb2984b3999726018cc9e59e0
出典メモuspto-grants-2013_02