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HRID 487268作成日:2026年10月26日

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

https://huagongshe.com/reaction/487268

反応式

関与物質

役割名称HCID仕込み量
反応物SodiumHCID 5360545—
反応物Ethyl imidazo[1,2-a]pyridine-6-carboxylateHCID 11830209—
反応物5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
溶媒EthanolHCID 702—
生成物1-cyclopentyl-3-ethyl-6-imidazo[1,2-a]pyridin-6-yl-2H-pyrazolo[3,4-d]pyrimidin-4-oneHCID 17843783462%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05294612
出典データセットuspto-grants-1994_03
ORD IDord-19b4b463815840d1850298edd2de8c12
出典メモuspto-grants-1994_03