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HRID 3645作成日:2026年10月24日

Dimethylformamide → 5-(2-Ethoxybenzamido)-1-n-propylimidazole-4-carboxamide

https://huagongshe.com/ja/reaction/3645

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Oxalyl chlorideHCID 65578—
反応物2-Ethoxybenzoic acidHCID 67252—
反応物5-Amino-1-propyl-1H-imidazole-4-carboxamideHCID 12339105—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物5-(2-Ethoxybenzamido)-1-n-propylimidazole-4-carboxamideHCID 5371330977%

反応手順

Oxalyl chloride (1.74 g, 0.137 mol) was added dropwise to a stirred solution of 2-ethoxybenzoic acid (1.1 g, 0.00663 mol) and dimethylformamide (0.1 ml) in dichloromethane (20 ml) and the resulting mixture stirred at ambient temperature for 4 hours, then evaporated under vacuum. The residue was azeotroped with dichloromethane (2×20 ml), then added dropwise to a stirred solution of 5-amino-1-n-propylimidazole-4-carboxamide (0.9 g, 0.00536 mol) in pyridine (20 ml) The resulting solution was stirred at ambient temperature for 3 days, then evaporated under vacuum. The residue was dissolved in dichloromethane (50 ml), and the solution washed with 1N hydrochloric acid (30 ml), dried (Na2SO4) and evaporated under vacuum. Chromatography of the crude product on silica gel (15 g) using a methanol in dichloromethane elution gradient (2-6% methanol), followed by crystallisation from ethanol, gave the title compound as a colourless solid (1.3 g, 77%), m.p. 182°-184° C. Found: C,60.85; H,6.40; N,18.06. C16H20N4O3 requires C,60.74; H,6.37; N,17.71%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05734053
出典データセットuspto-grants-1998_03
ORD IDord-7a5e2995d24f4bac852bdb664f6ad601
出典メモuspto-grants-1998_03