돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58318생성일: 2026년 10월 26일

2-Ethyl butylamine → N-(2-Ethylbutyl)-2-(3-nitro-2-oxopyridin-1(2H)-yl)acetamide

https://huagongshe.com/reaction/58318

반응식

참여 물질

역할이름HCID투입량
반응물2-Ethyl butylamineHCID 12049—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물(3-nitro-2-oxopyridin-1(2H)-yl)acetic acidHCID 607739—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
용매DimethylformamideHCID 6228—
생성물N-(2-Ethylbutyl)-2-(3-nitro-2-oxopyridin-1(2H)-yl)acetamideHCID 89925698—

반응 단계

The crude product 2-(3-nitro-2-oxopyridin-1(2H)-yl)acetic acid (˜14.7 mmol), 4.71 g (14.7 mmol) of TBTU, 1.98 g (14.7 mmol) of HOBT and 4.99 mL (29.3 mmol, 2 eq) of DIPEA are dissolved in 60 mL of DMF (argon atmosphere). 1.97 mL (14.7 mmol) of 2-ethyl-butylamine ((→pH=6) and another eq DIPEA (→pH=8) are added. After 1 h a half eq DIPEA is further titrated and stirred overnight at RT. If the TLC control shows incomplete conversion, it is stirred for further 3 h at 45° C. The solvent is removed in vacuo and the residue is taken up in 500 mL of DCM/MeOH (8/2). It is subsequently washed with 10% citric acid (3×100 mL), saturated NaHCO3 solution (3×100 mL) and brine (75 mL). The organic phase is dried over sodium sulfate and the solvent is removed in vacuo. The crude product (3.5 g) is treated with 10 mL of ethyl acetate, 30 mL of PE (40-60) is added and stirred for 15 min at RT. The solid is filtered off, washed with some amount of PE and dried.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434763B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-d3572670c03c4663a3e38859d8f611d1
출처 메모uspto-grants-2016_09