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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40241생성일: 2026년 10월 24일

Sodium Bicarbonate → 6-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinazolin-4(3H)-one

https://huagongshe.com/ko/reaction/40241

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물3-Hydrazinyl-6-phenylpyridazineHCID 6409842—
반응물2-(4-Oxo-3,4-dihydroquinazolin-6-yl)acetic acidHCID 136026471—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물6-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinazolin-4(3H)-oneHCID 135987473—

반응 조건

온도150 °C

반응 단계

A mixture of 2-(4-oxo-3,4-dihydroquinazolin-6-yl)acetic acid (0.10 g, 0.5 mmol), 1-(6-phenylpyridazin-3-yl)hydrazine (0.1 g, 0.6 mmol) and p-toluenesulfonic acid monohydrate (0.09 g, 0.5 mmol) in 3 mL of dioxane was heated with microwave at 150° C. for 1 hour in a microwave tube. The mixture was diluted with 70 mL of EtOAc and 40 mL of satd. NaHCO3 solution. The organic phase was separated and was washed with 40 mL of brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (EtOAc to 15% MeOH/EtOAc) to give light yellow solid as desired product 6-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinazolin-4(3H)-one. MS (ESI, pos. ion) m/z: 355.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524900B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-0a32eec8b9eb4426b5067b6befb1011a
출처 메모uspto-grants-2013_09