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HRID 82720作成日:2026年10月26日

Diisopropylethylamine → 4-amino-N-(6-chloropyridin-2-yl)-1,2,5-oxadiazole-3-carboxamide

https://huagongshe.com/reaction/82720

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物2-Amino-6-chloropyridineHCID 206246—
反応物Sodium BicarbonateHCID 516892—
反応物4-Amino-1,2,5-oxadiazole-3-carboxylic acidHCID 547454—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
溶媒DimethylformamideHCID 6228—
生成物4-amino-N-(6-chloropyridin-2-yl)-1,2,5-oxadiazole-3-carboxamideHCID 58558321—

反応条件

温度25 °C

反応手順

A solution of 4-amino-1,2,5-oxadiazole-3-carboxylic acid (0.4 g, 3.1 mmol) and 6-chloropyridin-2-amine (0.56 g, 4.3 mmol) in N,N-dimethylformamide (6.2 mL) was treated with N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (1.4 g, 3.7 mmol) followed by N,N-diisopropylethylamine (0.76 mL, 4.3 mmol) at 0° C. The reaction mixture was stirred at 25° C. for 2 h, poured into saturated NaHCO3 (50 mL) and extracted with ethyl acetate (100 mL). The organic layer was separated and washed with brine (25 mL), dried with sodium sulfate, filtered, and concentrated to a crude solid. The crude solid was washed with ethyl acetate and filtered. The filtrate was concentrated and purified on silica gel to give the desired product with some impurities. The impurities were removed by washing the solid with chloroform to yield the desired product (65 mg, 9%). LCMS for C8H7ClN5O2 (M+H)+: m/z=240.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846726B2
出典データセットuspto-grants-2014_09
ORD IDord-f6d3c17003254f4097d6eb0e3f792084
出典メモuspto-grants-2014_09