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HRID 49846作成日:2026年10月24日

2-chloro-N-(4-chlorophenyl)pyridine-3-carboxamide → N-(4-Chlorophenyl)-2-[1-(4-pyridyl)piperidin-4-ylmethyl]aminopyridine-3-carboxamide

https://huagongshe.com/ja/reaction/49846

反応式

関与物質

役割名称HCID仕込み量
反応物2-chloro-N-(4-chlorophenyl)pyridine-3-carboxamideHCID 587906—
反応物[1-(Pyridin-4-yl)piperidin-4-yl]methanamineHCID 10607746—
溶媒TriethylamineHCID 8471—
生成物N-(4-Chlorophenyl)-2-[1-(4-pyridyl)piperidin-4-ylmethyl]aminopyridine-3-carboxamideHCID 1299057324%

反応手順

Using a similar procedure to that described in Example 8, Part B, 2-chloro-N-(4-chlorophenyl)pyridine-3-carboxamide (125 mg, 0.47 mmol), 1-(4-pyridyl)piperidin-4-ylmethylamine (90 mg, 0.47 mmol), and triethylamine (0.07 mL) yielded 40 mg (24%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710057B2
出典データセットuspto-grants-2004_03
ORD IDord-16505e1677fa44da9c425c98f1e22133
出典メモuspto-grants-2004_03