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HRID 492483作成日:2026年10月26日

Hydrogen Peroxide → 5-(4-Formylphenoxy)pyrazine-2-carboxamide

https://huagongshe.com/reaction/492483

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物Potassium CarbonateHCID 11430—
反応物5-(4-Formylphenoxy)pyrazine-2-carbonitrileHCID 59730110—
溶媒Dimethyl SulfoxideHCID 679—
溶媒DichloromethaneHCID 6344—
生成物5-(4-Formylphenoxy)pyrazine-2-carboxamideHCID 5973018847.4%

反応手順

Dissolve 5-(4-formylphenoxy)pyrazine-2-carbonitrile (1.87 g, 8.30 mmol) and K2CO3 (0.573 g, 4.15 mmol) in DMSO (21 mL). Add 30% H2O2 (2.4 mL, 20.8 mmol) and stir at room temperature for 22 hours. Add additional K2CO3 (0.573 g, 4.15 mmol) and heat at 55° C. for about 2.5 hours. Cool the reaction mixture and dilute with CH2Cl2 (200 mL). Wash with water (1× 100 mL) and saturated aqueous NaHCO3 (1× 100 mL). Dry the organic layer over Na2SO4, filter and concentrate. Purify by flash chromatography, eluting with 0-50% ethyl acetate in dichloromethane to give the title compound (0.478 g, 23.7%): TOF MS ES+ 244.1 (M+H)+, HRMS calcd for C12H10N3O3 244.0722 (M+H)+, found 244.0709, time 0.38 min; HPLC [YMC-Pack Pro C-18 (150×4.6 mm, S-5 microm), 0.1% TFA/acetonitrile in 0.1% TFA/water at 1.0 mL/min, 20-99% over 23 min], tR=7.2 min, 100% purity.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07531557B2
出典データセットuspto-grants-2009_05
ORD IDord-494e3cc8d3d14bed8a0778127e1c00f9
出典メモuspto-grants-2009_05