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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 655291생성일: 2026년 10월 25일

Imidazole → 3-Imidazol-1-yl-6-(6-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylmethyl)-quinoline

https://huagongshe.com/reaction/655291

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참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물Potassium CarbonateHCID 11430—
반응물L-ProlineHCID 145742—
반응물3-Bromo-6-(6-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylmethyl)-quinolineHCID 59320295—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Dimethyl SulfoxideHCID 679—
생성물3-Imidazol-1-yl-6-(6-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylmethyl)-quinolineHCID 5932025522%

반응 조건

온도120 °C

반응 단계

To a reaction vial was added 3-bromo-6-(6-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylmethyl)-quinoline (71 mg, 0.2 mmol, 1.0 equiv), CuI (7 mg, 0.04 mmol, 0.008 equiv), L-proline (9 mg, 0.08 mmol, 0.4 equiv) and K2CO3 (83 mg, 0.60 mmol, 3.0 equiv). The system was evacuated and filled with nitrogen (3×). A solution of degassed imidazole (27 mg, 0.4 mmol, 2.0 equiv) in DMSO (1 mL) was then added. The reaction was heated at 120° C. for 18 hours. The solvent was removed in vacuo and the residue absorbed onto silica gel and purified by flash chromatography (SiO2, CH2Cl2:CH3OH 100:0-90:10 to return the title compound (15 mg, 22% yield). Analytical data presented in Table 2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08071581B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-8113fd05a7594e8d9aa37e929998105d
출처 메모uspto-grants-2011_12