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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77281생성일: 2026년 10월 24일

2-Aminothiazole → 4-Iodo-N-(thiazol-2-yl)benzenesulfonamide

https://huagongshe.com/ko/reaction/77281

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물4-Iodobenzenesulfonyl chlorideHCID 7399—
반응물1,2,4-Thiadiazol-5-amine--hydrogen chloride (1/1)HCID 22014543—
용매PyridineHCID 1049—
생성물4-Iodo-N-(thiazol-2-yl)benzenesulfonamideHCID 101931838%

반응 단계

To a stirring solution of 2-aminothiazole (13.2 g, 132.2 mmol) and pyridine (20 mL) under N2, at 0° C., was added pipsyl chloride (20.0 g, 55.1 mmol). The mixture was stirred at ambient temperature for 17 hours. CH2Cl2/MeOH-2/1 (100 mL) was added. The mixture was filtered and the filtrate was purified via silica gel chromatography using 5% MeOH in CH2Cl2. The solid was triturated with CH2Cl2 to obtain the desired sulfonamide as a white solid (8.4 g, 20.9 mmol, 38% yield). 1H NMR (400 MHz, DMSO-d6) δ 12.83 (s, 1H), 7.94-7.90 (m, 2H), 7.57-7.54 (m, 2H), 7.26 (d, J=4.6 Hz, 1H), 6.86 (d, J=4.6 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841282B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9b26e25ad7924231ad93b93669dc473c
출처 메모uspto-grants-2014_09