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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 619144생성일: 2026년 10월 26일

4-(1H-imidazol-1-yl)benzaldehyde → HCID 178437849, 화합물

https://huagongshe.com/reaction/619144

반응식

참여 물질

역할이름HCID투입량
반응물4-(1H-imidazol-1-yl)benzaldehydeHCID 736530—
반응물5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
생성물HCID 178437849HCID 17843784994.4%

반응 조건

온도130 °C

반응 단계

A mixture of 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (1.18 g, 5.32 mmol), 4-(1-imidazolyl)benzaldehyde (1.37 g) and xylenes (8 ml) was warmed to 130° C. for 30 minutes, then to 160° C. for three days. The reaction mixture was cooled, and the product was collected by filtration and washed with Et2O to afford 1.88 g of 1-cyclopentyl-3-ethyl-6-[4-(1-imidazolyl)phenyl]pyrazolo[3,4-d]pyrimidin-4-one as the 6,7-saturated derivative. This derivative was mixed with ethanol (300 ml) and 30% H2O2 (3.0 ml) and refluxed overnight. Additional 30% H2O2 (3 ml) was added and the mixture was refluxed for 8 hours. An additional 10 ml of 30% H2O2 was added and the mixture was refluxed overnight. Starting material was still present so an additional 10 ml of 30% H2O2 was added and the mixture was refluxed for 4 hours and then additional 30% H2O2 (10 ml) was added and the mixture was stirred for 1 hour, then was allowed to stand at room temperature overnight. The reaction mixture was stripped to a yellow liquid and purified by column chromatography on silica gel eluting with ethyl acetate (100%), then 5% methanol/ethyl acetate to afford 0.4 g of 1-cyclopentyl-3-ethyl-6-[4-(1-imidazolyl)phenyl]-pyrazolo[3,4-d]pyrimidin-4-one 1/2 hydrate, m.p. >300° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05958929
출처 데이터셋uspto-grants-1999_09
ORD IDord-07327be4e6924d88a6c7ad5e59a6443f
출처 메모uspto-grants-1999_09