돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38246생성일: 2026년 10월 24일

Triethylamine → N-(3-methoxy-4-(pyrimidin-2-yloxy)phenyl)picolinamide

https://huagongshe.com/ko/reaction/38246

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Picolinoyl Chloride HydrochlorideHCID 135033—
반응물3-Methoxy-4-(pyrimidin-2-yloxy)anilineHCID 62110961—
용매DichloromethaneHCID 6344—
생성물N-(3-methoxy-4-(pyrimidin-2-yloxy)phenyl)picolinamideHCID 4264523819.1%

반응 단계

According to Scheme 3 Step 3: Picolinoyl chloride hydrochloride (1.33 mmol, 256 mg) and Et3N (2.67 mmol, 0.37 mL) were added sequentially to a solution of 3-methoxy-4-(pyrimidin-2-yloxy)aniline (0.89 mmol, 193 mg) in DCM (3 mL) at 0° C. The reaction mixture was stirred at room temperature for 2 hours. The organic phase was washed with a saturated solution of NaHCO3. The aqueous phase was extracted with AcOEt. The organic phase was washed with brine, was dried over MgSO4, was filtered and was concentrated under reduced pressure. The crude product was purified by flash chromatography over C18 column using water/ACN (70:30) as eluent to afford N-(3-methoxy-4-(pyrimidin-2-yloxy)phenyl)picolinamide (0.17 mmol, 55 mg, 19%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524726B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-a7f5fcf130d348a486c01d6789d738a7
출처 메모uspto-grants-2013_09