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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 963045생성일: 2026년 10월 25일

2-Naphthalenesulfonyl chloride → N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazol-3-ylmethyl)naphthalene-2-sulfonamide

https://huagongshe.com/reaction/963045

반응식

참여 물질

역할이름HCID투입량
반응물2-Naphthalenesulfonyl chlorideHCID 7125—
반응물TriethylamineHCID 8471—
반응물Sodium BicarbonateHCID 516892—
반응물3-Aminomethyl-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazole ditosylateHCID 19085095—
용매DimethylformamideHCID 6228—
생성물N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazol-3-ylmethyl)naphthalene-2-sulfonamideHCID 1908529522.1%

반응 단계

3-Aminomethyl-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazole di-p-toluenesulfonate (1.85 g) was dissolved in dimethylformamide (20 ml). 2-Naphthalenesulfonyl chloride (0.62 g) and triethylamine (1.75 ml) were added under ice-cooling, and the mixture was allowed to stand overnight. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated, and the residue was recrystallized from ethyl acetate to give 0.32 g of N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazol-3-ylmethyl)naphthalene-2-sulfonamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05760032
출처 데이터셋uspto-grants-1998_06
ORD IDord-451bdcc49b3e45b8b5b815ae8c7a12c5
출처 메모uspto-grants-1998_06