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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 547168생성일: 2026년 10월 27일

Potassium Carbonate → N-(4-chloro-2-fluorophenyl)-6-methoxy-7-[2-(pyrrolidin-1-yl)ethoxy]quinazolin-4-amine

https://huagongshe.com/reaction/547168

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-(2-Chloroethyl)pyrrolidine hydrochlorideHCID 81668—
반응물Pyrrolidine, hydrochloride (1:1)HCID 212848—
반응물4-(4-Chloro-2-fluorophenylamino)-7-hydroxy-6-methoxyquinazolineHCID 135513720—
용매DimethylformamideHCID 6228—
생성물N-(4-chloro-2-fluorophenyl)-6-methoxy-7-[2-(pyrrolidin-1-yl)ethoxy]quinazolin-4-amineHCID 532901810%

반응 조건

온도100 °C

반응 단계

1-2-Chloroethyl)pyrrolidine hydrochloride (200 mg, 1.2 mmol) was added to a mixture of 4-(4-chloro-2-fluoroanilino)-7-hydroxy-6-methoxyquinazoline (403 mg, 1.26 mmol), (prepared as described for the starting material in Example 2), and potassium carbonate (650 mg, 4.7 mmol) in DMF (4 ml). The mixture was heated to 100° C. and further portions of 1-(2-chloroethyl)pyrrolidine hydrochloride (800 mg in total) were added periodically over 4 hours while the reaction mixture was maintained at 100° C. The reaction was then allowed to cool and volatiles were removed by evaporation. The residue was partitioned between methylene chloride and water, separated and the organic phase passed through phase separating paper. Column chromatography eluting with methylene chloride/methanol (95/5) gave 4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-(pyrrolidin-1-yl)ethoxy)quinazoline (50 mg, 10%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE042353E1
출처 데이터셋uspto-grants-2011_05
ORD IDord-2494c1ce89174d669c97ecc127d586c6
출처 메모uspto-grants-2011_05