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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42225생성일: 2026년 10월 24일

Heptane → 1,4-dichloro-6-(4-methoxybenzyl)-6,7-dihydro-5H-pyrrolo[3,4-d]pyridazine

https://huagongshe.com/ko/reaction/42225

반응식

참여 물질

역할이름HCID투입량
반응물HeptaneHCID 8900—
반응물Sodium CarbonateHCID 10340—
반응물4-MethylbenzylamineHCID 66035—
반응물4,5-Bis(bromomethyl)-3,6-dichloropyridazineHCID 57471629—
촉매Tetrabutylammonium IodideHCID 67553—
용매TetrahydrofuranHCID 8028—
생성물1,4-dichloro-6-(4-methoxybenzyl)-6,7-dihydro-5H-pyrrolo[3,4-d]pyridazineHCID 5924053641%

반응 조건

온도70 °C

반응 단계

To a suspension of 4,5-bis(bromomethyl)-3,6-dichloropyridazine (800 mg, 2.39 mmol) in 40 mL anhydrous THF was added with sodium carbonate (507 mg, 4.78 mmol) and tetrabutylammonium iodide (88.3 mg, 0.24 mmol). The reaction mixture was added with 4-methylbenzylamine (0.31 mL, 2.39 mmol) in 20 mL THF dropwisely for 2 h. The reaction mixture was heated at 70° C. for 8 h and concentrated. The crude material was dissolved in DCM and washed with water and brine. The organic solution was dried over Na2SO4 and concentrated to afford a crude oil. The mixture was purified by flash chromatography on silica gel, eluting with 10-80% EtOAc:heptane to afford a off-white solid (300 mg, yield: 41%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536168B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-5a00fc92a557426b89643e8e79018b9c
출처 메모uspto-grants-2013_09