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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 589896생성일: 2026년 10월 26일

Triethylamine → 1-{4-[(2-Aminoimidazo[1,2-b]pyridazin-6-yl)ethynyl]phenyl}-3-(3-methylphenyl)urea

https://huagongshe.com/reaction/589896

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물6-Iodoimidazo[1,2-B]pyridazin-2-amineHCID 57441024—
반응물1-(4-Ethynylphenyl)-3-(3-methylphenyl)ureaHCID 118638434—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
생성물1-{4-[(2-Aminoimidazo[1,2-b]pyridazin-6-yl)ethynyl]phenyl}-3-(3-methylphenyl)ureaHCID 118638414—

반응 단계

To a nitrogen bubbled solution of 6-iodo-imidazo[1,2-b]pyridazin-2-ylamine (260 mg, 1 mmol, 1 eq) and 1-(4-ethynylphenyl)-3-(3-methylphenyl)urea (375 mg, 1.5 eq) in DMF (5 mL) was added triethylamine (0.56 mL, 4 eq), bis(triphenylphosphine)palladium(II) dichloride (70.2 mg, 0.1 eq), and copper(I) iodide (38.1 mg, 0.2 eq). The reaction mixture was stirred at room temperature for 10 minutes and then partitioned between saturated aq NaHCO3 and i-PrOH—CHCl3 (1:4). The aqueous layer was extracted once more with i-PrOH—CHCl3 (1:4). The two organic layers were combined, washed with brine, and dried with anhydrous Na2SO4. The upper clear liquid was decanted, concentrated with silica gel, and the solid mixture was chromatographed (eluted from DCM to MeOH-DCM 1:15). The product fractions were collected and concentrated. The solid residue was triturated with EtOAc-Hex (1:1) and gave 1-{4-[(2-aminoimidazo[1,2-b]pyridazin-6-yl)ethynyl]phenyl}-3-(3-methylphenyl)urea as a brown solid upon filtration in amount of 133 mg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09233968B1
출처 데이터셋uspto-grants-2016_01
ORD IDord-23b537517f624047ab6905b106169cff
출처 메모uspto-grants-2016_01