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HRID 1416265생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1416265

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물6-Bromo-2-(chloromethyl)imidazo[1,2-a]pyridineHCID 11622894—
반응물Piperazine, 1-(4-chlorophenyl)-, hydrochloride (1:2)HCID 12212341—
용매Ethylene GlycolHCID 174—
생성물6-Bromo-2-[[4-(4-chlorophenyl)-1-piperazinyl]methyl]imidazo[1,2-a]pyridineHCID 19367128—

반응 조건

온도80 °C

반응 단계

A mixture of 6-bromo-2-(chloromethyl)imidazo[1,2-α]pyridine (Example 15, Step 1; 0.3042 g), 1-(4-chlorophenyl)piperazine dihydrochloride (Aldrich; 0.3708 g), triethylamine (Aldrich; 0.55 mL), and ethylene glycol (5.6 mL) is stirred for 1 h at 80° C. After cooling, the mixture is partitioned between water and dichloromethane. The combined organic layers are washed with brine, dried with MgSO4, and concentrated under reduced pressure. The residue is chromatographed on silica gel using methanol/dichloromethane (4/96) to give, after crystallization from ethyl acetate/methanol/dichlormetane, 0.1756 g of the title compound; mp 154-155° C.; MS m/z 404, 406, 408; IR (mineral oil) 1495, 1500, 1224, 823, 812 cm-1 ; 1H NMR (CDCl3) δ2.72, 3.19, 3.76, 6.83, 7.20, 7.22, 7.47, 7.52, 8.24.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05912246
출처 데이터셋uspto-grants-1999_06
ORD IDord-94e86b75667d4d1f9cf7e59f8190eb74
출처 메모uspto-grants-1999_06