戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2065042作成日:2026年10月27日

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

https://huagongshe.com/reaction/2065042

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4-(2-Methyl-[1,3]dioxolan-2-yl)-2-(3-nitro-pyrazol-1-ylmethyl)-thiazoleHCID 66929144—
触媒IronHCID 23925—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物1-[4-(2-Methyl-[1,3]dioxolan-2-yl)-thiazol-2-ylmethyl]-1H-pyrazol-3-ylamineHCID 66928995—

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 4-(2-methyl-[1,3]dioxolan-2-yl)-2-(3-nitro-pyrazol-1-ylmethyl)-thiazole (320 mg, 1.08 mmol), iron powder (183 mg, 3.24 mmol) and NH4Cl (292 mg, 5.40 mmol) in a mixture of EtOH (2.0 mL) and water (1.0 mL) was stirred at 75° C. for 60 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (10 mL) was added followed by 1N NaOH (10 mL). The aq. layer was extracted with CH2Cl2 (2×10 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 brown oil. LC-MS-conditions 01: tR=0.54 min; [M+H]+=266.97.

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-62d488c2fea1457c87d186fa06fdc6e4
出典メモuspto-grants-2012_10