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HRID 375116作成日:2026年10月25日

Triethylamine → 2-[4-(3-Hydroxy-2-sulfobenzoyl)amino-1H-imidazol-1-yl]octanoic acid

https://huagongshe.com/reaction/375116

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl 2-(4-nitro-1H-imidazole-1-yl)octanoateHCID 10062368—
反応物3-Hydroxy-2-sulfobenzoic acidHCID 13669120—
反応物ethyl 2-(4-amino-1H-imidazol-1-yl)octanoateHCID 15222343—
触媒DimethylformamideHCID 6228—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
溶媒Oxalyl chlorideHCID 65578—
生成物2-[4-(3-Hydroxy-2-sulfobenzoyl)amino-1H-imidazol-1-yl]octanoic acidHCID 15222327—

反応手順

2-Carboxy-6-hydroxybenzenesulfonic acid (1.8 mmole, 400 mg) was dissolved in 15 ml of oxalyl chloride. One drop of DMF was added. The reaction was stirred for 30 minutes at room temperature. The solvent was removed in vacuo, and 20 ml THF added. A solution of ethyl 2-(4-amino-1H-imidazol-1-yl)octanoate (prepared by the reduction of 1.8 mmoles of ethyl 2-(4-nitro-1H-imidazol-1-yl)octanoate in ethanol with 5% Pd/C) in 40 ml THF and 2.0 mmoles of triethylamine was added dropwise. The reaction was stirred at room temperature for 3 hours; ethyl acetate was added. The solution was washed with water, dried over sodium sulfate and concentrated. The intermediate was slurried in ether, filtered, chromatographed over silica gel eluted with 15% methanol in methylene chloride. The ester was hydrolyzed in 20 ml methanol and 45 ml of 2N NaOH at room temperature for 2 hours. The solvent was removed; water was added. The pH was adjusted to 2.0 using 5N HCL. The product was extracted into ethyl acetate, dried over sodium sulfate and concentrated to yield 2-[4-(3-Hydroxy-2-sulfobenzoyl)amino-1H-imidazol-1-yl]octanoic acid. (MS)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05484780
出典データセットuspto-grants-1996_01
ORD IDord-66d9ee9263fc4a17b3f1b1b9155f1a18
出典メモuspto-grants-1996_01