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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238962생성일: 2026년 10월 26일

1-Hydroxybenzotriazole hydrate → 1-[4-Chloro-2-(trifluoromethyl)phenyl]-5-[2-(dimethylamino)-2-oxoethyl]-2-methyl-N-[4-(methylsulfonyl)phenyl]-1H-pyrrole-3-carboxamide

https://huagongshe.com/reaction/238962

반응식

참여 물질

역할이름HCID투입량
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물Dimethylamine tetrahydrofuranHCID 22320367—
반응물(1-[4-chloro-2-(trifluoromethyl)phenyl]-5-methyl-4-{[4-(methylsulfonyl)phenyl]carbamoyl}-1H-pyrrol-2-yl)acetic acidHCID 67376656—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물1-[4-Chloro-2-(trifluoromethyl)phenyl]-5-[2-(dimethylamino)-2-oxoethyl]-2-methyl-N-[4-(methylsulfonyl)phenyl]-1H-pyrrole-3-carboxamideHCID 4527918454%

반응 단계

To a solution of the above (1-[4-chloro-2-(trifluoromethyl)phenyl]-5-methyl-4-{[4-(methylsulfonyl)phenyl]carbamoyl}-1H-pyrrol-2-yl)acetic acid (30 mg, 0.518 mmol) in DMF (0.58 mL), 1-hydroxybenzotriazole monohydrate (18 mg, 0.12 mmol) and hydrochloric acid 1-(3-dimethyl-aminopropyl)-3-ethylcarbodiimide (23 mg, 0.12 mmol) were successively added, and the mixture was stirred at room temperature for 1 hour. Thereafter, a 2M dimethylamine/THF solution was added to the mixture, and the mixture was stirred overnight. After the reaction, it was diluted with ethyl acetate, and the organic layer was washed with 1M hydrochloric acid, water and saturated brine. Thereafter, it was dried with sodium sulfate, filtration was carried out, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (17 mg, 54%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642640B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-32ca8c75f39c49a292aee21de54de583
출처 메모uspto-grants-2014_02