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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 522884생성일: 2026년 10월 24일

Dimethylformamide → 3-(4-(4-(3,4-Dimethyl-phenyl)piperazin-1-yl)-1,3,5-triazin-2-ylamino)-2-methylbenzamide

https://huagongshe.com/ko/reaction/522884

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물2,4-Dichloro-1,3,5-triazineHCID 17810—
반응물DiisopropylethylamineHCID 81531—
반응물1-(3,4-Xylyl)piperazineHCID 2723782—
반응물3-Amino-2-methylbenzamideHCID 16495773—
반응물3-(4-Chloro-1,3,5-triazin-2-ylamino)-2-methylbenzamideHCID 86685246—
용매WaterHCID 962—
생성물3-(4-(4-(3,4-Dimethyl-phenyl)piperazin-1-yl)-1,3,5-triazin-2-ylamino)-2-methylbenzamideHCID 6737573156%

반응 조건

온도0 °C

반응 단계

To a solution of 2,4-dichloro-1,3,5-triazine (50.0 mg, 0.333 mmol) in DMF (1334 μL, 0.333 mmol) was added N-ethyl-N-isopropylpropan-2-amine (174 μL, 1.000 mmol). The reaction mixture was cooled in an ice-water bath prior to the addition of 3-amino-2-methylbenzamide (50.1 mg, 0.333 mmol). The reaction mixture was stirred for 1 h at 0° C. at which time LC-MS revealed complete conversion to 3-(4-chloro-1,3,5-triazin-2-ylamino)-2-methylbenzamide. To this yellow solution was added 1-(3,4-dimethylphenyl)piperazine (63.4 mg, 0.333 mmol). The reaction mixture was allowed to stir and warm slowly to RT over 3 h. Water was added yielding a precipitate, which was filtered off, washed with water, and then purified further by reverse phase liquid chromatography using TFA as a modifier. Fractions containing the product were combined and washed with sat. NaHCO3. The product was extracted with CH2Cl2. The organic phase was washed with brine, dried over MgSO4, filtered, and concentrated to afford 3-(4-(4-(3,4-dimethyl-phenyl)piperazin-1-yl)-1,3,5-triazin-2-ylamino)-2-methylbenzamide (78 mg, 0.187 mmol, 56.0% yield) was obtained as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09334269B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-64143ab4d2c042caa894239489221090
출처 메모uspto-grants-2016_05