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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58315생성일: 2026년 10월 25일

2-Ethyl butylamine → Benzyl-1-(2-(2-ethylbutylamino)-2-oxoethyl)-2-oxo-1,2-dihydropyridin-3-yl-carbamate

https://huagongshe.com/reaction/58315

반응식

참여 물질

역할이름HCID투입량
반응물2-Ethyl butylamineHCID 12049—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물2-(3-(((Benzyloxy)carbonyl)amino)-2-oxopyridin-1(2H)-yl)acetic acidHCID 18672159—
용매DimethylformamideHCID 6228—
생성물Benzyl-1-(2-(2-ethylbutylamino)-2-oxoethyl)-2-oxo-1,2-dihydropyridin-3-yl-carbamateHCID 118104219—

반응 단계

A mixture of 3.70 g of 2-(3-(benzyloxycarbonylamino)-2-oxopyridin-1(2H)-yl)acetic acid (˜11.2 mmol), 3.58 g of TBTU (11.2 mmol), 1.51 g of HOBt (11.2 mmol) is dissolved in 60 mL of DMF. By addition of 5.70 mL of DIPEA (33.5 mmol, 3 eq) a pH value is adjusted to ˜10. 1.50 mL of 2-ethyl-butylamine (11.2 mmol) is added and the mixture is stirred at RT overnight. The solvent is removed in vacuo and the obtained residue is taken up in 300 mL of DCM and subsequently washed with 10% citric acid (3×75 mL), saturated NaHCO3 solution (3×75 mL) and brine (75 mL). The organic phase is dried over Na2SO4, filtered and concentrated in dryness. Pale brown solid is obtained and it is suitable for further processing without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434763B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-95502cae39944280b66e93911e468eb4
출처 메모uspto-grants-2016_09