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HRID 487248作成日:2026年10月24日

Methanesulfonic Acid → HCID 178437841、化合物

https://huagongshe.com/ja/reaction/487248

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物6-Methyl-2-pyridinecarboxaldehydeHCID 70737—
反応物5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
生成物HCID 178437841HCID 17843784153.3%

反応手順

1-Cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (2.0 g, 9.0 mmol), 6-methyl-2-pyridinecarboxaldehyde (2.2 g, 18.0 mmol), methanesulfonic acid (0.5 ml) and xylenes (80 ml) were combined and heated to reflux for 24 hours. The solvents were removed in vacuo, ethanol was added and the solvents were removed in vacuo. The residue was partitioned between 10% K2CO3 and chloroform, the organic layer was separated and the aqueous layer was extracted with chloroform (3×200 ml). The combined organic layers were concentrated in vacuo, redissolved in dichloromethane and combined with silica gel (40 g). The slurry was air dried for 3 hours, and placed on a silica gel column (150 g). Elution with ether and concentration of the solvent in vacuo and drying the residue at 40° C. in high vacuum for 6 hours afforded 1.55 g (53%) of 1-cyclopentyl-3-ethyl-6-(6-methyl-2-pyridyl)-pyrazolo[3,4-d]pyrimidin-4-one.

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-36920c4b9c2e4c60843c0856108c7a55
出典メモuspto-grants-1994_03