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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 658478생성일: 2026년 10월 24일

Triethylamine → 4-chloro-N-methoxy-N-methylpyridine-2-carboxamide

https://huagongshe.com/ko/reaction/658478

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물N,N-dimethylhydroxylamine hydrochlorideHCID 27969—
반응물4-Chloropyridine-2-carbonyl chloride--hydrogen chloride (1/1)HCID 22397270—
용매AcetonitrileHCID 6342—
용매TetrahydrofuranHCID 8028—
생성물4-chloro-N-methoxy-N-methylpyridine-2-carboxamideHCID 5351081498%

반응 조건

온도0 °C

반응 단계

To a mixture of dimethylhydroxylamine HCl (510 mg, 5.18 mmol) and triethylamine (2.16 mL, 15.5 mmol) in anhydrous THF (9.41 mL) and acetonitrile (2.35 mL) was added 4-chloropyridine-2-carbonyl chloride hydrochloride (1.00 g, 4.71 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 2 h then at RT for 16 h. The solvent was removed under reduced pressure and partitioned between EtOAc and water. The organic layer was washed with H2O and brine, dried over Na2SO4, and concentrated under reduced pressure. The crude product was purified by MPLC (biotage) eluted with 30% EtOAc/Hex to afford 925 mg (98%) of 4-chloro-N-methoxy-N-methylpyridine-2-carboxamide as an orange oil: TLC (50% EtOAc/Hex), Rf=0.31.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08076488B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-8bf6eaa704a24a61b72f12afc0af72b6
출처 메모uspto-grants-2011_12