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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1597878생성일: 2026년 10월 26일

Benzene → HCID 178466938, 화합물

https://huagongshe.com/reaction/1597878

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물WaterHCID 962—
반응물4-(Diethylamino)-2-ethoxybenzaldehydeHCID 958708—
반응물5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
촉매PalladiumHCID 23938—
촉매p-Toluenesulfonic acid monohydrateHCID 521998—
용매HexaneHCID 8058—
생성물HCID 178466938HCID 17846693815.8%

반응 단계

A mixture of 2-ethoxy-4-(diethylamino)benzaldehyde (7.87 g, 35.56 mmol), 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (3.95 g, 17.78 mmol), p-toluenesulfonic acid monohydrate (0.05 g), 10% palladium on carbon (0.11 g) and benzene (150 ml) was refluxed overnight with the azeotropic removal of water. The catalyst was removed by filtration, and the filtrate was concentrated in vacuo. The residue was combined with that from a similar experimental run, and dissolved in CH2Cl2, and loaded onto a silica gel column. Elution of the column with ether/hexane (60/40) afforded a green foam which was titurated with refluxing hexane, and cooled and the product, as pale yellow needles, was collected by filtration to afford 1.19 g (8%) of 1-cyclopentyl-3-ethyl-6-[2-ethoxy-4-(diethylamino)phenyl]pyrazolo[3,4-d]pyrimidin-4-one, m.p. 138°-139° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05736548
출처 데이터셋uspto-grants-1998_04
ORD IDord-99927a1a151947c7b17a9b1760151020
출처 메모uspto-grants-1998_04