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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69176생성일: 2026년 10월 23일

Sec-Butylamine → sec-Butyl-(3-quinolin-6-ylmethyl-imidazo[1,2-b]pyridazin-6-yl)-amine

https://huagongshe.com/ko/reaction/69176

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참여 물질

역할이름HCID투입량
반응물Sec-ButylamineHCID 24874—
반응물Potassium FluorideHCID 522689—
반응물6-(6-Chloro-imidazo[1,2-b]pyridazin-3-ylmethyl)-quinolineHCID 57917446—
용매Ethyl AcetateHCID 8857—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물sec-Butyl-(3-quinolin-6-ylmethyl-imidazo[1,2-b]pyridazin-6-yl)-amineHCID 44208575—

반응 조건

온도180 °C

반응 단계

6-(6-Chloro-imidazo[1,2-b]pyridazin-3-ylmethyl)-quinoline (Example 14, 70 mg, 0.237 mmol), KF (70 mg, 1.187 mmol) and sec-butylamine (484 μL, 4.75 mmol) were suspended in NMP (1 mL). The RM was stirred at 180° C. for 29 h. The mixture was diluted with EtOAc and washed with 1 M Na2CO3 (×1) and water (×2). The aqueous was further extracted with EtOAc (2×). The combined organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography (Flashmaster) and then crystallized in Et2O to afford the title compound as a beige solid (tR 4.28 min (conditions 4), MH+ 332.3, 1H-NMR in DMSO-d6: 8.83 (m, 1H); 8.25 (m, 1H); 7.92 (d, 1H); 7.83 (m, 1H); 7.70 (m, 1H); 7.61 (d, 1H); 7.48 (dd, 1H); 7.32 (s, 1H); 6.66 (d, 1H); 6.56 (d, 1H); 4.34 (s, 2H); 3.70 (m, 1H); 1.46 (m, 2H); 1.07 (d, 3H); 0.80 (t, 3H)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822468B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-5f151d11ce1f41bfaabc1b24c412ecbb
출처 메모uspto-grants-2014_09