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HRID 1526597作成日:2026年10月27日

Dimethylformamide → Methyl 5-(thiazol-4-ylmethoxy)pyrazine-2-carboxylate

https://huagongshe.com/reaction/1526597

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Cesium carbonateHCID 10796—
反応物Methyl 5-chloropyrazine-2-carboxylateHCID 406081—
反応物(1,3-Thiazol-4-yl)methanolHCID 2763215—
溶媒WaterHCID 962—
生成物Methyl 5-(thiazol-4-ylmethoxy)pyrazine-2-carboxylateHCID 9038932142.2%

反応条件

温度40 °C

反応手順

A RBF was charged with methyl 5-chloropyrazine-2-carboxylate (1.239 g, 7.18 mmol, Ark Pharm), thiazol-4-ylmethanol (0.8266 g, 7.18 mmol), cesium carbonate (0.689 ml, 8.61 mmol, Alfa Aesar) and DMF (20.51 ml). The reaction mixture was stirred at 40° C. for 3 days. The reaction mixture was allowed to cool to rt and was diluted with water and extracted with EtOAc. The organic extract was washed with water, satd NaCl, dried over MgSO4, and concentrated in vacuo. The crude product was adsorbed onto a plug of silica gel and purified by silica gel flash chromatography, eluting with a gradient of 10% to 100% EtOAc in hexane, to provide methyl 5-(thiazol-4-ylmethoxy)pyrazine-2-carboxylate (0.7606 g, 3.03 mmol, 42.2% yield). MS m/z=252.1 [M+H]+. Calculated for C10H9N3O3S: 251.036. 1H NMR (400 MHz, DMSO-d6) δ ppm 3.89 (s, 2H) 5.60 (s, 1H) 7.86 (d, J=1.96 Hz, 1H) 8.46 (d, J=1.37 Hz, 1H) 8.86 (d, J=1.37 Hz, 1H) 9.14 (d, J=1.96 Hz, 1H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09085576B2
出典データセットuspto-grants-2015_07
ORD IDord-c0801f5801694ff6a152d83ac632dbb4
出典メモuspto-grants-2015_07