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HRID 655837作成日:2026年10月26日

1-(4-Nitrophenyl)-1h-pyrazolo[3,4-d]pyrimidin-4-amine → 1-(4-Amino-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamine

https://huagongshe.com/reaction/655837

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Nitrophenyl)-1h-pyrazolo[3,4-d]pyrimidin-4-amineHCID 221075—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物1-(4-Amino-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamineHCID 11995960—

反応手順

Title compound 10A, 1-(4-nitro-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamine (1.0 g, 3.9 mmol) was added to 10% w/w palladium on carbon (0.1 g, 10% w/w) suspended in ethanol (300 ml). This was stirred for 42 hours at room temperature under an atmosphere of hydrogen. The reaction mixture was filtered to remove the palladium residues and the filtrate was concentrated to dryness in vacuo. The resultant residue was purified by column chromatography using DCM/MeOH (96:4) as eluent to yield the title compound as an off-white solid. (0.53 g, 2.3 mmol, 60%). LCMS: [M+H]+=227, Rt=0.64 min, 100% purity.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08071607B2
出典データセットuspto-grants-2011_12
ORD IDord-3d56aac5c1494b83bbf004dc23b2879e
出典メモuspto-grants-2011_12