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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 619184생성일: 2026년 10월 27일

Benzene → HCID 178466938, 화합물

https://huagongshe.com/reaction/619184

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 번호US05958929
출처 데이터셋uspto-grants-1999_09
ORD IDord-7d482d272b9042e3b034bf1175e482ee
출처 메모uspto-grants-1999_09