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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2374423생성일: 2026년 10월 25일

Potassium Iodide → 4-(5-Chloro-2,3-methylenedioxypyrid-4-ylamino)-6-methoxy-7-[3-(4-prop-2-ynylpiperazin-1-yl)propoxy]quinazoline

https://huagongshe.com/reaction/2374423

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물1-(2-Propynyl)piperazineHCID 14627369—
반응물4-(5-Chloro-2,3-methylenedioxypyrid-4-ylamino)-7-(3-chloropropoxy)-6-methoxyquinazolineHCID 68548521—
용매DimethylacetamideHCID 31374—
생성물4-(5-Chloro-2,3-methylenedioxypyrid-4-ylamino)-6-methoxy-7-[3-(4-prop-2-ynylpiperazin-1-yl)propoxy]quinazolineHCID 984924068.3%

반응 조건

온도80 °C

반응 단계

A mixture of 4-(5-chloro-2,3-methylenedioxypyrid-4-ylamino)-7-(3-chloropropoxy)-6-methoxyquinazoline (0.08 g), 1-prop-2-ynylpiperazine (0.047 g), potassium iodide (0.01 g) and DMA (2 ml) was stirred and heated to 80° C. for 3.5 hours. The solvent was evaporated and the residue was partitioned between methylene chloride and a saturated aqueous ammonium chloride solution. The organic phase was dried over magnesium sulphate and evaporated. The residue was purified by column chromatography on silica using a 19:1 mixture of methylene chloride and methanol and then a 9:1 mixture of methylene chloride and a saturated methanolic ammonia solution as eluent. The resulting gum was triturated under diethyl ether. There was thus obtained the title compound as a solid (0.066 g); NMR Spectrum: (DMSOd6 and CF3CO2D) 2.3 (m, 2H), 3.2-3.6 (br m, 10H), 3.75 (s, 1H), 3.95 (br s, 2H), 4.0 (s, 3H), 4.35 (m, 2H), 6.3 (s, 2H), 7.4 (s, 1H), 7.9 (s, 1H), 8.15 (s, 1H), 8.95 (s, 1H); Mass Spectrum: M+H+ 511 and 513.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07462623B2
출처 데이터셋uspto-grants-2008_12
ORD IDord-fadac8a8289843d596ed7cac4873929f
출처 메모uspto-grants-2008_12