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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1519667생성일: 2026년 10월 25일

Diisopropylethylamine → 4-((t-Butoxycarbonyl)(methyl)amino)-4'-(((2-methoxy-1-((methylamino)carbonyl)-2-oxoethyl)(methyl)amino)carbonyl)biphenyl

https://huagongshe.com/reaction/1519667

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물4'-((t-Butoxycarbonyl)(methyl)amino)biphenyl-4-carboxylic acidHCID 71268254—
반응물N,N2,O-trimethyl-3-oxoserinamide hydrochlorideHCID 86679246—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물4-((t-Butoxycarbonyl)(methyl)amino)-4'-(((2-methoxy-1-((methylamino)carbonyl)-2-oxoethyl)(methyl)amino)carbonyl)biphenylHCID 7126821351%

반응 단계

N,N2,O-trimethyl-3-oxoserinamide hydrochloride (Intermediate 5-2, 90 mg), HATU (0.17 g) and DIPEA (0.16 mL) were added to a DMF (2.0 mL) solution of 4′-((t-butoxycarbonyl)(methyl)amino)biphenyl-4-carboxylic acid (0.10 g), as obtained in Example 2-(2), and the mixture was stirred for 16 hours at room temperature. Ethyl acetate and water were added to the reaction mixture to isolate the organic layer, and the extract was washed sequentially with water and brine. The system was dried over anhydrous sodium sulfate and, after separation of the desiccant by filtration, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/3) to obtain 4-((t-butoxycarbonyl)(methyl)amino)-4′-(((2-methoxy-1-((methylamino)carbonyl)-2-oxoethyl)(methyl)amino)carbonyl)biphenyl (white foam) (73 mg, 51%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09073821B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-4a328d5ec0564b43ab762dfde2cd9f1b
출처 메모uspto-grants-2015_07