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HRID 1416258作成日:2026年10月25日

Triethylamine → 6-Chloro-2-[[4-(3-chlorophenyl)-1-piperazinyl]methyl]-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1416258

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物6-Chloro-2-(chloromethyl)imidazo[1,2-a]pyridineHCID 4868389—
反応物1-(3-Chlorophenyl)piperazine dihydrochlorideHCID 11957487—
溶媒Ethylene GlycolHCID 174—
生成物6-Chloro-2-[[4-(3-chlorophenyl)-1-piperazinyl]methyl]-imidazo[1,2-a]pyridineHCID 1936715858.5%

反応手順

Following the general procedure of Example 11 and making noncritical variations, 6-chloro-2-(chloromethyl)imidazo[1,2-a]pyridine (Example 4, Step 1; 0.354 g), 1-(3-chlorophenyl)piperazine dihydrochloride (Aldrich; 0.475 g), triethylamine (0.552 g), and ethylene glycol (2 mL) give 0.372 g of the title compound after chromatography (silica gel, methanol/dichloromethane, 4/96) and crystallization from dichloromethane/hexane; mp 148-149° C.; MS m/z 360; IR (mineral oil) 1594, 1340, 1073, 1218, 1502 cm-1. 1H NMR (CDCl3) δ2.71, 3.23, 3.76, 6.79, 6.86, 7.14, 7.52, 7.53, 8.14.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05912246
出典データセットuspto-grants-1999_06
ORD IDord-5eb213c044c2400aacc5a115b1d9772f
出典メモuspto-grants-1999_06