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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1384642생성일: 2026년 10월 26일

Potassium Carbonate → 4-(4-Chloro-2-fluoroanilino)-6-methoxy-7-(2-(3-pyridyloxy)ethoxy)quinazoline

https://huagongshe.com/reaction/1384642

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-(2-Chloroethoxy)pyridine hydrochlorideHCID 22624985—
반응물4-(4-Chloro-2-fluorophenylamino)-7-hydroxy-6-methoxyquinazolineHCID 135513720—
용매WaterHCID 962—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물4-(4-Chloro-2-fluoroanilino)-6-methoxy-7-(2-(3-pyridyloxy)ethoxy)quinazolineHCID 2262490921.5%

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온도90 °C

반응 단계

A mixture of 4-(4-chloro-2-fluoroanilino)-7-hydroxy-6-methoxyquinazoline (350 mg, 1.0 mmol), (prepared as described for the starting material in Example 24), 3-(2-chloroethoxy)pyridine hydrochloride (234 mg, 1.2 mmol) and potassium carbonate (456 mg, 3.3 mmol) in NMP (20 ml) was heated at 90° C. for 2 hours. The mixture was allowed to cool, diluted with water and extracted with ethyl acetate. The combined extracts were washed with water, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/methanol mixtures (100/0 increasing to 95/5) to give 4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-(3-pyridyloxy)ethoxy)quinazoline (95 mg, 20%). m.p. 188-190° C. 1H NMR Spectrum: (DMSOd6) 3.90(s, 3H); 4.45(m, 4H); 7.24(s, 1H); 7.18(dd, 1H); 7.2-7.60(m, 3H); 7.80(s, 1H); 8.20(d, 1H); 8.35(s, 2H); 9.50(s, 1H) MS-ESI: 441 [MH]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06258951B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-bc30baebc4aa45b385ddec7a86266854
출처 메모uspto-grants-2001_07