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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 401556생성일: 2026년 10월 25일

Triethylamine → N-(5-Methylpyridin-2-yl)pivalamide

https://huagongshe.com/reaction/401556

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Amino-5-methylpyridineHCID 15348—
반응물Pivaloyl chlorideHCID 62493—
용매DichloromethaneHCID 6344—
생성물N-(5-Methylpyridin-2-yl)pivalamideHCID 418292498.4%

반응 단계

To a stirred solution of 5-methylpyridin-2-amine (200 g, 1.85 mol) in anhydrous CH2Cl2 (1000 mL) was added dropwise a solution of Et3N (513 mL, 3.70 mol) and 2,2-dimethyl-propionyl chloride (274 mL, 2.22 mol) at 0° C. under N2. The ice bath was removed and stirring was continued at room temperature for 2 hours. The reaction was poured into ice (2000 g). The organic layer was separated and the remaining aqueous layer was extracted with CH2Cl2 (3×). The combined organics were dried over Na2SO4 and evaporated to afford 2,2-dimethyl-N-(5-methyl-pyridin-2-yl)-propionamide (350 g), which was used in the next step without further purification. 1H NMR (400 MHz, CDCl3) δ 8.12 (d, J=8.4 Hz, 1H), 8.06 (d, J=1.2 Hz, 1H), 7.96 (s, 1H), 7.49 (dd, J=1.6, 8.4 Hz, 1H), 2.27 (s, 1H), 1.30 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741933B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-5dfb903e7c3f434494b3e1a1ded8f230
출처 메모uspto-grants-2014_06