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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2411226생성일: 2026년 10월 23일

Diisopropylethylamine → HCID 71252181, 화합물

https://huagongshe.com/ko/reaction/2411226

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물N,N-bis(2-chloroethyl)-p-toluenesulphonamideHCID 96039—
반응물4,6-Dimethylpyridin-3-amineHCID 7060669—
용매WaterHCID 962—
생성물HCID 71252181HCID 7125218115.7%

반응 단계

To 5-amino-2,4-dimethylpyridine (883 mg) were added N,N-diisopropylethylamine (2.1 mL) and N,N-bis(2-chloroethyl)-p-toluenesulfonamide (2.08 g), and the mixture was stirred with heating under reflux. After completion of the reaction, water was added to the reaction mixture, the mixture was extracted with chloroform, and the solvent was evaporated. The obtained residue was purified by column chromatography (chloroform:methanol) to give 1-(4,6-dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazine (380 mg). The obtained 1-(4,6-dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazine (380 mg) was dissolved in acetic acid (2 mL), 40% hydrobromic acid (2 mL) was added, and the mixture was stirred at 100° C. After completion of the reaction, the reaction mixture was neutralized with aqueous sodium hydroxide solution, and the mixture was extracted with ethyl acetate. The solvent was evaporated from the organic layer to give the title compound (131 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08816079B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-eb0674f3edd244f3995b85e2b604a5a1
출처 메모uspto-grants-2014_08