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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 487268생성일: 2026년 10월 24일

Sodium → 1-cyclopentyl-3-ethyl-6-imidazo[1,2-a]pyridin-6-yl-2H-pyrazolo[3,4-d]pyrimidin-4-one

https://huagongshe.com/ko/reaction/487268

반응식

참여 물질

역할이름HCID투입량
반응물SodiumHCID 5360545—
반응물Ethyl imidazo[1,2-a]pyridine-6-carboxylateHCID 11830209—
반응물5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
용매EthanolHCID 702—
생성물1-cyclopentyl-3-ethyl-6-imidazo[1,2-a]pyridin-6-yl-2H-pyrazolo[3,4-d]pyrimidin-4-oneHCID 17843783462%

반응 단계

Sodium metal (0.21 g, 9.2 mmol) was dissolved in ethanol (25 ml) and 6-carboethoxyimidazo[1,2-a]pyridine (1.75 g, 9.2 mmol) and 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (1.02 g, 4.6 mmol) were added. The reaction mixture was heated to reflux for 24 hours, cooled to room temperature and stirred for 60 hours. The solvent was removed in vacuo, the residue was dissolved in water (100 ml) and the solution was neutralized by the addition of concentrated HCl. A precipitate was obtained which was collected by filtration through a glass frit. The solid was recrystallized from ethanol and washed with ether to afford 0.98 g (62%) of 1-cyclopentyl-3-ethyl-6-(6-imidazo[1,2-a]pyridinyl)-pyrazolo[3,4-d]pyrimidin-4-one as white crystals, m.p. >300° C. when dried for 18 hours at 120° C. in high vacuum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05294612
출처 데이터셋uspto-grants-1994_03
ORD IDord-19b4b463815840d1850298edd2de8c12
출처 메모uspto-grants-1994_03