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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2250700생성일: 2026년 10월 25일

Pyridine → 5-Methyl-thiophene-2-carboxylic acid (7-bromo-4-methoxybenzothiazol-2-yl)-amide

https://huagongshe.com/reaction/2250700

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물5-Methylthiophene-2-carbonyl chlorideHCID 2760083—
반응물7-Bromo-4-methoxy-1,3-benzothiazol-2-amineHCID 22283200—
용매DichloromethaneHCID 6344—
생성물5-Methyl-thiophene-2-carboxylic acid (7-bromo-4-methoxybenzothiazol-2-yl)-amideHCID 86584910—

반응 단계

2-Amino-7-bromo-4-methoxybenzothiazol (2.33 g, 9 mmol) is dissolved in dichloromethane (100 ml) and at 0° C. treated with pyridine (2.2 ml, 27 mmol) and 5-methyl-thiophene-2-carbonyl chloride (2.2 g, 13.5 mmol). The reaction mixture is allowed to warm to room temperature and after stirring for additional 18 h quenched with water (100 ml). After separation of the phases, the aqueous phases are extracted twice with ethyl acetate. The combined organic layers are then washed with brine, dried and avaporated to dryness. Flash chromatography on silica (eluent ethyl acetate/cyclohexane 1:1 to 4:1) and final recrystallization from ethyl acetate affords the product as off-white solid. (34 mg, 69%). MS: m/e=384 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07317007B2
출처 데이터셋uspto-grants-2008_01
ORD IDord-fba67789ff78464ca8329f1fb3615320
출처 메모uspto-grants-2008_01