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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58320생성일: 2026년 10월 24일

Isoamylamine → Benzyl 1-(2-(isopentylamino)-2-oxoethyl)-2-oxo-1,2-dihydropyridin-3-ylcarbamate

https://huagongshe.com/ko/reaction/58320

반응식

참여 물질

역할이름HCID투입량
반응물IsoamylamineHCID 7894—
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-(isopentylamino)-2-oxoethyl)-2-oxo-1,2-dihydropyridin-3-ylcarbamateHCID 89926023—

반응 단계

A mixture of 900 mg of 2-(3-(benzyloxycarbonylamino)-2-oxopyridin-1(2H)-yl)acetic acid (˜2.32 mmol), 744 mg of TBTU (2.32 mmol), 313 mg of HOBt (2.32 mmol) is dissolved in 25 mL of DMF. By addition of 985 μL of DIPEA (5.79 mmol, 2.5 eq) a pH value is adjusted to ˜9. 539 μL of isopentylamine (4.63 mmol) is added and the mixture is stirred at RT for 2.5 h. The solvent is removed in vacuo and the obtained residue is taken up in 100 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 vacuo in dryness. Brown solid is obtained and it is suitable for further processing without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434763B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-4c59b1cf2fb54ed2b9e9e6ffdabb5b8f
출처 메모uspto-grants-2016_09