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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 843648생성일: 2026년 10월 26일

Water → 2-[3-(2-Chlorophenyl)-6-fluoro-4-oxo-3,4-dihydroquinazolin-2-yl-vinyl)pyridine-2-carbaldehyde

https://huagongshe.com/reaction/843648

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1,4-DioxaneHCID 31275—
반응물4(3H)-Quinazolinone, 3-(2-chlorophenyl)-6-fluoro-2-methyl-HCID 64065—
반응물2,6-DiformylpyridineHCID 79485—
촉매ZincchlorideHCID 3007855—
용매Acetic AnhydrideHCID 7918—
생성물2-[3-(2-Chlorophenyl)-6-fluoro-4-oxo-3,4-dihydroquinazolin-2-yl-vinyl)pyridine-2-carbaldehydeHCID 86583867—

반응 단계

A catalytic amount (about 100 mg) of anhydrous zinc chloride was added to a solution of 576 mg (2.0 mmol) of 3-(2-chlorophenyl)-6-fluoro-2-methyl-4(3H)-quinazolinone and 270 mg (2.0 mmol) of 2,6-pyridinedicarboxaldehyde in 20-25 mL of dioxane and 1.0 mL of acetic anhydride. The reaction mixture was heated at reflux under a nitrogen atmosphere for 3 hours until TLC indicated that the starting materials had been consumed. The cooled reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The combined extracts were dried with brine and magnesium sulfate, treated with decolonizing carbon and filtered and the solvent was removed to give the desired product. This was taken up in 2:1 ether/pentane and the crystals were filtered to give 266 mg of the product, 33%, m.p. 247-248° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06380204B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-e414f10c31ef4c24873d9551f513cbb0
출처 메모uspto-grants-2002_04