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HRID 2383792作成日:2026年10月27日

1,2-Diaminocyclohexane, trans- → 5-(3-Naphthalen-2-yl-2-oxo-imidazolidin-1-yl)-nicotinic Acid Methyl Ester

https://huagongshe.com/reaction/2383792

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Diaminocyclohexane, trans-HCID 43806—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Methyl 5-bromopyridine-3-carboxylateHCID 699336—
反応物1-Naphthalen-2-yl-imidazolidin-2-oneHCID 59636167—
触媒Copper iodideHCID 83717—
溶媒1,4-DioxaneHCID 31275—
生成物5-(3-Naphthalen-2-yl-2-oxo-imidazolidin-1-yl)-nicotinic Acid Methyl EsterHCID 5963624726.99%

反応手順

Using the same reaction conditions as in Example 79, 1-naphthalen-2-yl-imidazolidin-2-one (I-79b: 100 mg, 0.4711 mmol) was reacted with 5-bromo-nicotinic acid methyl ester (112 mg, 0.5182 mmol), 1,4-dioxane (10 mL), copper iodide (11 mg), trans-1,2-diamino cyclohexane (22 mg) and potassium phosphate (200 mg, 0.9422 mmol) to afford the crude product. Purification by column chromatography on silica gel (80% EtOAc in hexane) afforded 44 mg of the product (26.99% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08263635B2
出典データセットuspto-grants-2012_09
ORD IDord-635fc8d43aea4c16a4115df560e7503d
出典メモuspto-grants-2012_09