戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 644209作成日:2026年10月23日

2-amino-N-(5-chloropyridin-2-yl)benzamide → 2-[4-(B enzyloxy)-2-(1-tert-butoxycarbonylpiperidin-4-yloxy)benzoylamino]-N-(5-chloropyridin-2-yl)benzamide

https://huagongshe.com/ja/reaction/644209

反応式

関与物質

役割名称HCID仕込み量
反応物2-amino-N-(5-chloropyridin-2-yl)benzamideHCID 21906381—
反応物4-Benzyloxy-2-(1-tert-butoxycarbonylpiperidin-4-yloxy)benzoic acidHCID 68535719—
生成物2-[4-(B enzyloxy)-2-(1-tert-butoxycarbonylpiperidin-4-yloxy)benzoylamino]-N-(5-chloropyridin-2-yl)benzamideHCID 68532666—

反応手順

Using methods substantially equivalent to those described in Example 1-F, 4-benzyloxy-2-(1-tert-butoxycarbonylpiperidin-4-yloxy)benzoic acid (529 mg, 1.27 mmol) and N-(5-chloropyridin-2-yl)-2-aminobenzamide (297 mg, 1.20 mmol) afforded, after purification by chromatography (SiO2: EtOAc in hexanes), 493 mg (63%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07700628B2
出典データセットuspto-grants-2010_04
ORD IDord-b362c472deaa453eac5060bc7a1ee1e1
出典メモuspto-grants-2010_04