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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81946생성일: 2026년 10월 25일

Iodine → ethyl 8-iodo-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate

https://huagongshe.com/reaction/81946

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Isoamyl NitriteHCID 8053—
반응물Cesium iodideHCID 24601—
반응물ethyl 8-amino-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylateHCID 24993827—
촉매Copper iodideHCID 83717—
용매1,2-DimethoxyethaneHCID 8071—
생성물ethyl 8-iodo-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylateHCID 4423294346%

반응 단계

To a well stirred suspension of ethyl 8-amino-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate (9.0 g, 33 mmol) in dimethoxyethane (0.7 L) under N2, cesium iodide (8.6 g, 33 mmol), bisublimated iodine (4.19 g, 16.5 mmol), copper iodide (2.0 g, 10 mmol) and isopentyl nitrite (6.62 mL, 49.5 mmol) were added in sequence. The reaction mixture was stirred vigorously at 65-70° C. for 3 hours. After cooling in an ice-water bath, the solid was filtered off. The filtrate was diluted with dichloromethane (2.0 L), washed with 30% ammonium hydroxide (150 mL), sodium thiosulphate (300 mL), brine, dried over anhydrous Na2SO4 and concentrated to give 5.69 g of the title compound (46% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846701B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-bc92d3892c64466fa8b33352c03f5173
출처 메모uspto-grants-2014_09