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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 398690생성일: 2026년 10월 24일

Pyridine → 2-(3-chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-N-(2-methyl-pyrimidin-4-yl)-propionamide

https://huagongshe.com/ko/reaction/398690

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Oxalyl chlorideHCID 65578—
반응물2-Methylpyrimidin-4-amineHCID 295763—
반응물2-(3-Chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acidHCID 12067654—
촉매DimethylformamideHCID 6228—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2-(3-chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-N-(2-methyl-pyrimidin-4-yl)-propionamideHCID 2231515625%

반응 조건

온도0 °C

반응 단계

A solution of 2-(3-chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acid (200 mg, 0.61 mmol) in methylene chloride (2 mL) was treated with N,N-dimethylformamide (1 drop) and then cooled to 0° C. The reaction mixture was then treated dropwise with a 2M solution of oxalyl chloride in methylene chloride (0.45 mL, 0.91 mmol) and stirred at 0° C. for 30 min. The resulting reaction mixture was then treated with a solution of 4-amino-2-methylpyrimidine (98.9 mg, 0.91 mmol) and pyridine (0.25 mL, 3.03 mmol) in N,N-dimethylformamide (5 mL). The resulting reaction mixture was allowed to warm to 25° C. where it was stirred for 16 h. The reaction mixture was then diluted with water (10 mL) and extracted with ethyl acetate (3×15 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Biotage chromatography (FLASH 40S, Silica, 55/45 hexanes/ethyl acetate) afforded 2-(3-chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-N-(2-methyl-pyrimidin-4-yl)-propionamide (64 mg, 25%) as a colorless oil: EI-HRMS m/e calcd for C20H24ClN3O3S (M+) 421.1227, found 421.1230.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610846B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-5de6ffa36b4940d98dfbf4d942fd1755
출처 메모uspto-grants-2003_08