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HRID 78579作成日:2026年10月26日

1,1'-Carbonyldiimidazole → 3-amino-6-(4-(4-(dimethylamino)piperidine-1-carbonyl)phenyl)-N-phenylpyrazine-2-carboxamide

https://huagongshe.com/reaction/78579

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物DiisopropylethylamineHCID 81531—
反応物N,N-Dimethylpiperidin-4-amineHCID 417391—
反応物4-(5-Amino-6-(phenylcarbamoyl)pyrazin-2-yl)benzoic acidHCID 46833744—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒Dimethyl SulfoxideHCID 679—
生成物3-amino-6-(4-(4-(dimethylamino)piperidine-1-carbonyl)phenyl)-N-phenylpyrazine-2-carboxamideHCID 5947179580%

反応条件

温度38 °C

反応手順

N,N-dimethylpiperidin-4-amine (57.54 mg, 0.449 mmol) was weighed into a greenhouse tube and treated with a solution of 4-(5-amino-6-(phenylcarbamoyl)pyrazin-2-yl)benzoic acid (50 mg, 0.150 mmol), CDI (48.51 mg, 0.299 mmol) and DMAP (1.82 mg, 0.015 mmol) in DMSO (1 mL of a stock solution). DIPEA (78.2 uL, 0.449 mmol) was then added and the mixture stirred at 38° C. for 6 hours. The reaction mixture was filtered and the resultant residue was purified by reverse phase preparative HPLC [Waters Sunfire C18, 10 uM, 100 A column, gradient 10%-95% B (solvent A: 0.05% TFA in water, solvent B: CH3CN) over 16 minutes at 25 mL/min]. The fractions were freeze-dried to give the title compound as a solid (54.65, 80% Yield). (ES+) 445

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841308B2
出典データセットuspto-grants-2014_09
ORD IDord-fd646289a5c7410abe8cf54d7bb1968f
出典メモuspto-grants-2014_09