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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1845229생성일: 2026년 10월 26일

Diisopropylethylamine → N3,4'-Dimethyl-N5-((6-methylpyridin-3-yl)methyl)-N3-(pyridin-4-yl)biphenyl-3,5-dicarboxamide

https://huagongshe.com/reaction/1845229

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-(Methylamino)pyridineHCID 123098—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물4'-Methyl-5-((6-methylpyridin-3-yl)methylcarbamoyl)biphenyl-3-carboxylic acidHCID 58188051—
용매DimethylformamideHCID 6228—
생성물N3,4'-Dimethyl-N5-((6-methylpyridin-3-yl)methyl)-N3-(pyridin-4-yl)biphenyl-3,5-dicarboxamideHCID 58188202—

반응 조건

온도25 °C

반응 단계

To a solution of 4′-methyl-5-((6-methylpyridin-3-yl)methylcarbamoyl)-biphenyl-3-carboxylic acid (50 mg, 0.134 mmol) in N,N-dimethylformamide (1 mL) were added N-methylpyridin-4-amine (40 mg, 0.37 mmol), N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (120 mg, 0.32 mmol) and N,N-diisopropylethylamine (120 μL, 0.69 mmol). The reaction mixture was stirred for 16 hours at 25° C. The reaction mixture was purified by preparative HPLC to afford the final product as a light color solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08946439B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-648ab5c304614b94af63e29779fb5a6f
출처 메모uspto-grants-2015_02