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HRID 2064968作成日:2026年10月25日

Nitrogen → 1-[6-(2-Methyl-[1,3]dioxolan-2-yl)-pyridin-2-ylmethyl]-1H-pyrazol-4-ylamine

https://huagongshe.com/reaction/2064968

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2-(2-Methyl-[1,3]dioxolan-2-yl)-6-(4-nitro-pyrazol-1-ylmethyl)-pyridineHCID 66928936—
触媒IronHCID 23925—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物1-[6-(2-Methyl-[1,3]dioxolan-2-yl)-pyridin-2-ylmethyl]-1H-pyrazol-4-ylamineHCID 66928767—

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 0.1M solution of 2-(2-methyl-[1,3]dioxolan-2-yl)-6-(4-nitro-pyrazol-1-ylmethyl)-pyridine (145 mg, 0.50 mmol), iron powder (84 mg, 1.50 mmol) and NH4Cl (135 mg, 2.50 mmol) in a mixture of EtOH (2.0 mL) and water (1.0 mL) was stirred at 75° C. for 30 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (20 mL) was added followed by 1N NaOH (20 mL). The aq. layer was extracted with CH2Cl2 (2×20 mL) and 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=0.56 min; [M+H]+=261.61.

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-da875732ca6e4a119eb6f40ecc12f5db
出典メモuspto-grants-2012_10