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HRID 15991作成日:2026年10月27日

Sodium Nitrite → 6-bromo-1-(2,3-dihydro-benzofuran-5-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazine

https://huagongshe.com/reaction/15991

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium NitriteHCID 23668193—
反応物6-bromo-N2-(2,3-dihydro-benzofuran-5-ylmethyl)-pyrazine-2,3-diamineHCID 59341860—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物6-bromo-1-(2,3-dihydro-benzofuran-5-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazineHCID 5934184452.4%

反応手順

To a solution of 6-bromo-N2-(2,3-dihydro-benzofuran-5-ylmethyl)-pyrazine-2,3-diamine (1.0 g, 3.12 mmol) in AcOH:H2O (8 mL: 8 mL) was added the solution of NaNO2 (2.12 g, 31.2 mmol) in water (5 mL). The mixture was stirred at room temperature for 1 hour, and then heated at 65° C. for 16 hours. The solvents were removed, and then EtOAc (20 mL) and water (20 mL) were added. The aqueous layer was extracted with EtOAc (3×20 mL). The combined extracts were dried over Na2SO4, concentrated and purified by silica gel chromatography with EtOAc: Hexanes to provide 6-bromo-1-(2,3-dihydro-benzofuran-5-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazine (543 mg, 52% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732604B2
出典データセットuspto-grants-2010_06
ORD IDord-360d4cf41c634868a6a397e84190bdae
出典メモuspto-grants-2010_06