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HRID 2040054作成日:2026年10月26日

Nitrogen → 1-(5-((4-Amino-2H-1,2,3-triazol-2-yl)methyl)furan-2-yl)ethanone

https://huagongshe.com/reaction/2040054

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-(4-Nitro-[1,2,3]triazol-2-ylmethyl)-furan-2-yl]-ethanoneHCID 67127846—
触媒IronHCID 23925—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物1-(5-((4-Amino-2H-1,2,3-triazol-2-yl)methyl)furan-2-yl)ethanoneHCID 67127836—

反応条件

温度85 °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-((4-nitro-2H-1,2,3-triazol-2-yl)methyl)furan-2-yl)ethanone (WO2009077990A1) (500 mg, 2.12 mmol), iron powder (358 mg, 6.35 mmol) and NH4Cl (572 mg, 10.59 mmol) in a mixture of EtOH (8.0 mL) and water (4.0 mL) was stirred at 85° C. for 30 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (15 mL) was added followed by 1N NaOH (15 mL). The aq. layer was extracted with CH2Cl2 (2×15 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 yellow oil. LC-MS-conditions 02: tR=0.64 min; [M+H]+=207.49.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08580831B2
出典データセットuspto-grants-2013_11
ORD IDord-c77ff3d1f39a4f208f5933787b0d1061
出典メモuspto-grants-2013_11