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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1416293생성일: 2026년 10월 26일

Triethylamine → 6-Bromo-2-[[4-(2,4-dichlorophenyl)-1-piperazinyl]methyl]-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1416293

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-(2,4-Dichlorophenyl)piperazineHCID 2737527—
반응물6-Bromo-2-(chloromethyl)imidazo[1,2-a]pyridineHCID 11622894—
용매TetrahydrofuranHCID 8028—
생성물6-Bromo-2-[[4-(2,4-dichlorophenyl)-1-piperazinyl]methyl]-imidazo[1,2-a]pyridineHCID 19367124—

반응 조건

온도80 °C

반응 단계

A mixture of 6-bromo-2-(chloromethyl)imidazo[1,2-a]pyridine (Example 15, Step 1; 0.582 g), 1-(2,4-dichlorophenyl)piperazine (Example 31, Step 1; 0.548), triethylamine (Aldrich; 0.288 g), and THF (5 mL) is stirred at 80° C. for 6 h, at which time it is cooled and then partitioned between dichloromethane and aq. sodium bicarbonate. The organic layers are dried over sodium sulfate and concentrated. Chromatography of the residue on silica gel using methanol/dichloromethane (2/98) and crystallization gives 0.710 g of the title compound; mp 137-138° C.; MS m/z 438, 440; IR (mineral oil) 1479, 1341, 1058, 2810, 803 cm-1. 1H NMR (CDCl3) δ2.78, 3.09, 3.80, 6.96, 7.16-7.23, 7.35, 7.48, 7.55, 8.24.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05912246
출처 데이터셋uspto-grants-1999_06
ORD IDord-e85312339b5a4fbbaac35fb43cdd60ce
출처 메모uspto-grants-1999_06