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HRID 1029563作成日:2026年10月26日

Butyric Acid → 5-Butyramido-2-propylimidazo[4,5-b]pyridine

https://huagongshe.com/reaction/1029563

反応式

関与物質

役割名称HCID仕込み量
反応物Butyric AcidHCID 264—
反応物DichloromethaneHCID 6344—
反応物2,6-Diamino-3-nitropyridineHCID 319998—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒Ammonium HydroxideHCID 14923—
生成物5-Butyramido-2-propylimidazo[4,5-b]pyridineHCID 2240738149.1%

反応条件

温度80 °C

反応手順

A mixture of 2,6-diamino-3-nitropyridine (878 mg, 5.7 mmol) and Pd-C (10%, 100 mg) in MeOH (100 mL) was stirred under 1 atm. H2 for 16 hours. The mixture (containing the air sensitive triamine) was filtered, evaporated, and to this flask was added polyphosphoric acid (15 mL) and butyric acid (1.05 mL, 11.5 mmol). This mixture was heated to 80° C. for 5 hours, cooled to room temperature, diluted with water and neutralized with concentrated NH4OH. Extractive workup (CH2Cl2) gave 345 mg of 5-(butyramido)-2-propylimidazo[4,5-b]pyridine: 1H NMR (300 MHz, CDCl3) δ7.94 (d, 1H, J=8.5 Hz), 7.65 (d, 1H, J=8.5 Hz), 2.96 (t, 2H J=7.5 Hz), 2.30 (t, 2H J=7 Hz), 1.98-1.84 (m, 2H), 1.68-1.55 (m, 2H), 0.99 (t, 3H, J=7.5 Hz), 0.80 (t, 3H, J=7.0 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05102880
出典データセットuspto-grants-1992_04
ORD IDord-4ed784dc78a24cd2938997a23c8937e8
出典メモuspto-grants-1992_04