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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226022생성일: 2026년 10월 25일

Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → 8-(1-Ethyl-propyl)-2,6-dimethyl-3-(5-methoxy-3-methyl-benzo[b]thiophen-2-yl)-imidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/226022

반응식

참여 물질

역할이름HCID투입량
반응물Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
반응물Potassium methoxideHCID 23664618—
반응물8-(1-Ethyl-propyl)-2,6-dimethyl-3-(5-fluoro-3-methyl-benzo[b]thiophen-2-yl)-imidazo[1,2-b]pyridazineHCID 57752599—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물8-(1-Ethyl-propyl)-2,6-dimethyl-3-(5-methoxy-3-methyl-benzo[b]thiophen-2-yl)-imidazo[1,2-b]pyridazineHCID 57752684293.2%

반응 단계

In an oven dried, nitrogen purged, 3 neck, 50 mL round bottom flask, 0.014 g (0.197 mmol) of potassium methoxide and 0.005 mL (0.013 mmol) of tris[2-(2-methoxyethoxy)ethyl]amine are heated at 150° C. and stirred vigorously for 5 minutes. 0.050 g (0.131 mmol) of 8-(1-ethyl-propyl)-2,6-dimethyl-3-(5-fluoro-3-methyl-benzo[b]thiophen-2-yl)-imidazo[1,2-b]pyridazine is added and the reaction is followed by TLC (2:1 Hexanes/Ethyl Acetate) and MS. After 4 h, the reaction mixture is diluted with 20 mL dichloromethane and 20 mL of water. The layers are separated and the aqueous is extracted 3×50 mL of dichloromethane, dried (MgSO4), and concentrated under vacuum. The crude mixture is purified by chromatography using hexanes:ethyl acetate as a solvent system. Combined fractions to obtain 0.015 g of the title compound, 29% yield. MS, ES+=394.2 (M+1); H1NMR (DMSO-d6) δ 7.863-7.842 (d, J=8.368, 1H); 7.327-7.321 (m, 1H); 7.076-7.049 (m, 1H); 6.991 (s, 1H); 3.857 (s, 3H); 3.094 (m, 1H); 2.477 (s, 3H); 2.350 (s, 3H); 2.180 (s, 3H); 1.853-1.760 (m, 4H); 0.793-0.757 (m, 6H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557103B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-9379509429b54bf1ae38a798032173f3
출처 메모uspto-grants-2009_07