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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2055095생성일: 2026년 10월 25일

Pyrrolidine → 3-[2-Methyl-5-(2-pyrrolidin-1-ylpyrid-4-ylcarbonylamino)phenyl]-6-(4-methylpiperazin-1-yl)-3,4-dihydroquinazolin-4-one

https://huagongshe.com/reaction/2055095

반응식

참여 물질

역할이름HCID투입량
반응물PyrrolidineHCID 31268—
반응물3-[5-(2-Chloropyrid-4-ylcarbonylamino)-2-methylphenyl]-6-(4-methylpiperazin-1-yl)-3,4-dihydroquinazolin-4-oneHCID 22238152—
용매WaterHCID 962—
생성물3-[2-Methyl-5-(2-pyrrolidin-1-ylpyrid-4-ylcarbonylamino)phenyl]-6-(4-methylpiperazin-1-yl)-3,4-dihydroquinazolin-4-oneHCID 22238203—

반응 조건

온도100 °C

반응 단계

A mixture of 3-[5-(2-chloropyrid-4-ylcarbonylamino)-2-methylphenyl]-6-(4-methylpiperazin-1-yl)-3,4-dihydroquinazolin-4-one (0.18 g) and pyrrolidine (2 ml) was stirred and heated to 100° C. for 16 hours. The mixture was cooled to ambient temperature and poured into water. The resultant solid was isolated, washed with water and dried under vacuum at 40° C. There was thus obtained the title compound (0.11 g); NMR Spectrum: (DMSOd6) 1.94-1.97 (m, 4H), 2.04 (s, 3H), 2.22 (s, 3H), 2.45-2.49 (m, 4H), 3.25-3.28 (m, 4H), 3.4-3.45 (m, 4H), 6.85 (s, 1H), 6.96 (d, 1H), 7.42 (d, 1H), 7.42 (d, 1H), 7.44 (s, 1H), 7.62 (s, 2H), 7.77-7.79 (m, 2H), 8.07 (s, 1H), 8.2 (s, 1H), 10.42 (s, 1H); Mass Spectrum: M+H+ 524.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07332483B2
출처 데이터셋uspto-grants-2008_02
ORD IDord-ea5416ad3ae6489aa783ccf7b10eb0f9
출처 메모uspto-grants-2008_02