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HRID 78585作成日:2026年10月26日

Triethylamine → 3-amino-6-bromo-N'-(phenylcarbonyl)pyrazine-2-carbohydrazide

https://huagongshe.com/reaction/78585

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物BenzoylhydrazineHCID 11955—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物3-Amino-6-bromopyrazine-2-carboxylic acidHCID 18521600—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-amino-6-bromo-N'-(phenylcarbonyl)pyrazine-2-carbohydrazideHCID 5947235573.5%

反応手順

TBTU (22.09 g, 68.80 mmol) and triethylamine (4.642 g, 6.394 mL, 45.87 mmol) were added to a suspension of 3-amino-6-bromo-pyrazine-2-carboxylic acid (10 g, 45.87 mmol) and benzohydrazide (7.494 g, 55.04 mmol) in DMF (100.0 mL) and the resulting solution stirred at ambient temperature for 48 hours and then poured into water (400 mL) with vigorous stirring. This was allowed to stir for 30 minutes, filtered and washed with water. The moist solid was dissolved in hot EtOAc, dried (MgSO4), filtered and concentrated in vacuo and the resultant solid dried under vacuum to give the desired product (11.34 g, 73% Yield). 1H NMR (400.0 MHz, DMSO) d 7.51 (2H, m), 7.61 (1H, m), 7.69 (2H, br s), 7.92 (2H, m), 8.44 (1H, s), 10.48 (1H, br s), 10.54 (1H, br s) ppm; MS (ES+) 338.01

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841308B2
出典データセットuspto-grants-2014_09
ORD IDord-cd25e745e6ad4c6c8a4d53b81cbc2ae8
出典メモuspto-grants-2014_09