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HRID 619150作成日:2026年10月26日

2-(2-Morpholinoethoxy)benzaldehyde → HCID 178437837、化合物

https://huagongshe.com/reaction/619150

反応式

関与物質

役割名称HCID仕込み量
反応物2-(2-Morpholinoethoxy)benzaldehydeHCID 976593—
反応物5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
生成物HCID 178437837HCID 178437837—

反応条件

温度120 °C

反応手順

A mixture of 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (0.95 g, 4.28 mmol), 2-[2-(4-morpholinyl)ethoxy]benzaldehyde (1.51 g) and xylenes (15 ml) was heated to 120° C. for 1 hour, then to 160° C. until the reaction was complete. The reaction mixture was then cooled to room temperature, the solvent was removed in vacuo, and the residue was purified by silica gel chromatography eluting with ethyl acetate (100%), followed by ethanol/ethyl acetate (1/1) to afford 1-cyclopentyl-3-ethyl-6-[2-[2-(4-morpholinyl)ethoxy]phenyl]pyrazolo[3,4-d]pyrimidin-4-one (Example 11 (b)), as an oil. The free base was then converted into its hydrochloride salt, which was recrystallized from ethanol and dried at 110° C. under high vacuum to afford 0.5 g of 1-cyclopentyl-3-ethyl-6-[2-[2-(4-morpholinyl)ethoxy]phenyl]pyrazolo[3,4-d]pyrimidin-4-one monohydrochloride, as an off-white powder, m.p. 235-237° C., labelled as Example 11 (c).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05958929
出典データセットuspto-grants-1999_09
ORD IDord-89cff62d6ad343639d13da68032ff3d2
出典メモuspto-grants-1999_09