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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226115생성일: 2026년 10월 25일

Ethyl N-methoxy-N-methylcarbamate → 3-(5-Fluoro-3-methyl-benzo[b]thiophen-2-yl)-2,6-dimethyl-imidazo[1,2-b]pyridazine-8-carboxylic acid methoxy-methyl-amide

https://huagongshe.com/reaction/226115

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl N-methoxy-N-methylcarbamateHCID 533715—
반응물Lithium diisopropylamideHCID 2724682—
반응물3-(5-Fluoro-3-methyl-benzo[b]thiophen-2-yl)-2,6-dimethyl-imidazo[1,2-b]pyridazineHCID 68859850—
용매TetrahydrofuranHCID 8028—
생성물3-(5-Fluoro-3-methyl-benzo[b]thiophen-2-yl)-2,6-dimethyl-imidazo[1,2-b]pyridazine-8-carboxylic acid methoxy-methyl-amideHCID 8662104531.7%

반응 조건

온도-78 °C

반응 단계

The solution of 3-(5-fluoro-3-methyl-benzo[b]thiophen-2-yl)-2,6-dimethyl-imidazo[1,2-b]pyridazine (2.09 g, 6.73 mmol) in THF (56 mL) is stirred at −78° C. Ethyl N-methoxy-N-methylcarbamate (4.48 g, 33.7 mmol) is added. LDA (10 mL, 20.1 mmol) is added dropwise to maintain reaction temperature at −75° C. The reaction is stirred at −78° C. for 1 hour. The mixture is quenched with H2O, filtered through celite with CH2Cl2. The collect solution is washed with H2O, dried over Na2SO4, filtered and concentrated. The crude is purified by ISCO (50-100% EtOAc/Hexane) to give the title compound (0.85 g, 31%). 1H NMR (CDCl3): δ 7.8 (dd, J=4.8, 8.5 Hz, 1H), 7.5 (dd, J=2.5, 9.7 Hz, 1H), 7.2 (m, 1H), 7.0 (s, 1H), 3.7 (s, 3H), 3.5 (s, 3H), 2.6 (s, 3H), 2.55 (s, 3H), 2.3 (s, 3H) ppm. MS (m/e): 399 (100%, M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557103B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-8fc792b35b1541978efcda4e44742859
출처 메모uspto-grants-2009_07