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HRID 70144作成日:2026年10月24日

Hydrochloric Acid → 5-Methyl[1,3]oxazolo[4,5-b]pyridine-2(3H)-thione

https://huagongshe.com/ja/reaction/70144

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Carbon DisulfideHCID 6348—
反応物Potassium HydroxideHCID 14797—
反応物6-Methyl-2-nitropyridin-3-olHCID 84801—
反応物Ammonium formateHCID 2723923—
触媒Palladium hydroxideHCID 9942167—
溶媒EthanolHCID 702—
生成物5-Methyl[1,3]oxazolo[4,5-b]pyridine-2(3H)-thioneHCID 12664278—

反応条件

温度70 °C

反応手順

Ammonium formate (1.64 g, 26 mmol) was added to a suspension of Pd(OH)2 on carbon (˜20% Pd, 0.73 g, 1.0 mmol) and 2-nitro-3-hydroxy-6-methylpyridine (2.0 g, 13 mmol) in EtOH (20 mL). The reaction mixture was heated to 70° C. for 1 h at which point the reaction mixture was allowed to cool to rt and was filtered through Celite®. The filtrate was concentrated under reduced pressure, yielding a thick orangish oil. The material was dissolved in EtOH (25 mL) and potassium hydroxide (0.875 g, 15.6 mmol) and carbon disulfide (15 mL) were added. The reaction mixture was heated to reflux overnight. Upon cooling to rt, the reaction mixture was acidified with 1 N HCl, and the resulting solid was collected by filtration. The solid was washed with water (2×) and air dried followed by drying in a 35° C. vacuum oven. LC-MS: RT=5.58 min, [M+H]+=167.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822472B2
出典データセットuspto-grants-2014_09
ORD IDord-64982537af614bce91986c2fc8093296
出典メモuspto-grants-2014_09