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HRID 1654842作成日:2026年10月25日

2-Amino-3-(2-bromobenzyloxy)pyridine → N'-[3-[(2-bromophenyl)methoxy]-2-pyridinyl]-2-phenylethanimidamide

https://huagongshe.com/reaction/1654842

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-3-(2-bromobenzyloxy)pyridineHCID 10468808—
反応物Ethyl 2-phenylacetimidate hydrochlorideHCID 12218775—
溶媒EthanolHCID 702—
生成物N'-[3-[(2-bromophenyl)methoxy]-2-pyridinyl]-2-phenylethanimidamideHCID 1785107923.5%

反応手順

A mixture of 2-amino-3-(2-bromobenzyloxy)pyridine (5.58 g, 20 mmol) and ethyl phenylacetimidate hydrochloride (4.39 g, 22 mmol) in ethanol (80 ml) was heated under reflux for 2 hours. Evaporation of the solvent gave a residue which was purified by chromatography (silica, chloroform/methanol) and recrystallisation from ethanol/ether to obtain the product (0.28 g), m.p. 158°-169° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05409943
出典データセットuspto-grants-1995_04
ORD IDord-0a3816cd36fe4debac1ed2ba97b645ff
出典メモuspto-grants-1995_04