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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11696생성일: 2026년 10월 24일

Triethylamine → N-[3-(3-{2-[4-(4-Fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-6-methyl-pyridin-2-yl)-propionyl]-methanesulfonamide

https://huagongshe.com/ko/reaction/11696

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물MethanesulfonamideHCID 72879—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물3-(3-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-6-methyl-pyridin-2-yl)-propionic acidHCID 69655226—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물N-[3-(3-{2-[4-(4-Fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-6-methyl-pyridin-2-yl)-propionyl]-methanesulfonamideHCID 6965577942.6%

반응 단계

To a solution of 3-(3-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-6-methyl-pyridin-2-yl)-propionic acid (0.10 g, 0.23 mmol) in methylene chloride (2 mL) was added 4-dimethylaminopyridine (0.032 g, 0.27 mmol), (3-(dimethylamino)propyl)ethyl carbodiimide hydrochloride (0.051 g, 0.27 mmol), methanesulfonamide (0.025 g, 0.27 mmol) and triethylamine (0.037 mL, 0.27 mmol). The reaction was stirred at ambient temperature for 18 hours. The reaction mixture was then diluted with dichloromethane and washed with 0.2 M hydrochloric acid. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The crude product was purified by chromatography on silica gel to give the title compound (0.051 g, LRMS: 521.5).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098212B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-63c48ff29cef4147bc2af082637a14cc
출처 메모uspto-grants-2006_08