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HRID 2204843作成日:2026年10月27日

Triethylamine → 4-(5-amino-6-(2-(6-aminopyridine-2-carbonyl)hydrazinecarbonyl)pyrazin-2-yl)-N,N-dimethylbenzamide

https://huagongshe.com/reaction/2204843

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物6-Aminopyridine-2-carboxylic acidHCID 351652—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物4-(5-amino-6-(hydrazinecarbonyl)pyrazin-2-yl)-N,N-dimethylbenzamideHCID 59471641—
溶媒DimethylformamideHCID 6228—
生成物4-(5-amino-6-(2-(6-aminopyridine-2-carbonyl)hydrazinecarbonyl)pyrazin-2-yl)-N,N-dimethylbenzamideHCID 59472227—

反応手順

A solution of 4-[5-amino-6-(hydrazinecarbonyl)pyrazin-2-yl]-N,N-dimethyl-benzamide (100 mg, 0.3163 mmol) and 6-aminopyridine-2-carboxylic acid (43.69 mg, 0.3163 mmol) in DMF (1.000 mL) weas treated with triethylamine (32.01 mg, 44.09 μL, 0.3163 mmol) then warmed slightly. The mixture was cooled to room temperature and then treated with (benzotriazol-1-yloxy-dimethylamino-methylene)-dimethyl-ammonium tetrafluoroborate (121.9 mg, 0.3796 mmol) and stirred at room temperature overnight. The mixture was poured dropwise onto water (5 ml) with rapid stirring, stirred at room temperature for 1 h then filtered to give a wet paste which was dried under high vacuum at 100° C. overnight. Used directly in the next step without purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09365557B2
出典データセットuspto-grants-2016_06
ORD IDord-bd6a801f443d4f73932e41f13583722b
出典メモuspto-grants-2016_06