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HRID 2064921作成日:2026年10月24日

Nitrogen → 1-[5-(2-Methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-4-ylamine

https://huagongshe.com/ja/reaction/2064921

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Ammonium ChlorideHCID 25517—
反応物1-[5-(2-Methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-4-nitro-1H-pyrazoleHCID 66928564—
触媒IronHCID 23925—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物1-[5-(2-Methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-4-ylamineHCID 66928611—

反応条件

温度75 °C

反応手順

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a mixture of 1-[5-(2-methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-4-nitro-1H-pyrazole (427 mg, 1.53 mmol), iron powder (258 mg, 4.59 mmol) and NH4Cl (413 mg, 7.65 mmol) in a mixture of EtOH (8.0 mL) and water (4.0 mL) was stirred at 75° C. for 2.5 h. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (30 mL) was added followed by 1M NaOH (30 mL). The aq. layer was extracted with CH2Cl2 (2×20 mL). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure to give the title compound as a deep red oil. LC-MS-conditions 02: tR=0.58 min; [M+H]+=250.4.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08288419B2
出典データセットuspto-grants-2012_10
ORD IDord-0951923b3d504c3ca7cdd9ccf2e90952
出典メモuspto-grants-2012_10