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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375116생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/375116

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl 2-(4-nitro-1H-imidazole-1-yl)octanoateHCID 10062368—
반응물3-Hydroxy-2-sulfobenzoic acidHCID 13669120—
반응물ethyl 2-(4-amino-1H-imidazol-1-yl)octanoateHCID 15222343—
촉매DimethylformamideHCID 6228—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매Oxalyl chlorideHCID 65578—
생성물2-[4-(3-Hydroxy-2-sulfobenzoyl)amino-1H-imidazol-1-yl]octanoic acidHCID 15222327—

반응 단계

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)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05484780
출처 데이터셋uspto-grants-1996_01
ORD IDord-66d9ee9263fc4a17b3f1b1b9155f1a18
출처 메모uspto-grants-1996_01