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HRID 1824504作成日:2026年10月27日

2-Amino-4-methylpyridine → 2-(4'-Chloropropoxy-3'-methoxyphenyl)-7-methylimidazo[1,2-a]pyridine hydrobromide

https://huagongshe.com/reaction/1824504

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-4-methylpyridineHCID 1533—
反応物alpha-Bromo-3'-methoxy-4'-chloropropoxyacetophenoneHCID 22015629—
溶媒EthanolHCID 702—
生成物2-(4'-Chloropropoxy-3'-methoxyphenyl)-7-methylimidazo[1,2-a]pyridine hydrobromideHCID 2201559870.5%

反応手順

A solution of the product of Step B (1.44 g) and 2-amino-4-picoline (0.486 g) in ethanol (6 mL) was heated at 73° C. for 1 hour. The reaction mixture was cooled to ambient temperature and evaporated to a yellow solid. The solid was stirred with 25 mL of dichloromethane for approximately 10 minutes. The mixture was filtered and the solid product collected to yield the title compound (1.3 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07041827B2
出典データセットuspto-grants-2006_05
ORD IDord-11c85a8ee7884795a73a6fb9892f0127
出典メモuspto-grants-2006_05