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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44627생성일: 2026년 10월 24일

Iodine → HCID 57444149, 화합물

https://huagongshe.com/ko/reaction/44627

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Isoamyl NitriteHCID 8053—
반응물Cesium iodideHCID 24601—
반응물8-amino-1-methyl-N-[(1S)-2-morpholin-4-yl-1-phenylethyl]-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamideHCID 57444150—
촉매Copper iodideHCID 83717—
용매1,2-DimethoxyethaneHCID 8071—
생성물HCID 57444149HCID 5744414940%

반응 단계

To a well stirred and warm suspension of 8-amino-1-methyl-N-[(1S)-2-morpholin-4-yl-1-phenylethyl]-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide (3 g, 6.92 mmol) in dimethoxyethane (240 mL), maintained in an inert atmosphere of argon, cesium iodide (2.16 g, 8.3 mmol), bisublimated iodine (870 mg, 3.46 mmol), copper iodide (460 mg, 2.42 mmol) and isopentyl nitrite (1.71 mL, 1.5 g, 12.46 mmol) were added, in sequence. The reaction mixture was stirred vigorously at 65-70° C. for 18 hours. After cooling in an ice-water bath, the solid was filtered off and the filtrate was diluted with dichloromethane (100 mL), washed with 30% ammonium hydroxide (50 mL), sodium thiosulphate (100 mL), brine and dried over anhydrous Na2SO4. The crude was purified by flash chromatography on silica gel (eluant: dichloromethane/methanol 95:59) and 1.48 g of the title compound was isolated (40% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541429B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-b27aceb55e484bbc8f9a5441de48ba65
출처 메모uspto-grants-2013_09