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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 859803생성일: 2026년 10월 27일

1-Hydroxybenzotriazole → N-(6-Methyl-4'-{[2-(4-methylpiperazin-1-ylmethyl)anilino]carbonyl}-1,1'-biphenyl-3-yl)-3-furamide

https://huagongshe.com/reaction/859803

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물2-[(4-Methylpiperazin-1-yl)methyl]anilineHCID 6484556—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물5'-(3-Furoylamino)-2'-methyl-1,1'-biphenyl-4-carboxylic acidHCID 69152146—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-(6-Methyl-4'-{[2-(4-methylpiperazin-1-ylmethyl)anilino]carbonyl}-1,1'-biphenyl-3-yl)-3-furamideHCID 69152273—

반응 단계

5′-(3-Furoylamino)-2′-methyl-1,1′-biphenyl-4-carboxylic acid (50 mg, 0.156 mmol), 2-(4-methylpiperazin-1-ylmethyl)aniline (32.0 mg, 0.156 mmol), HATU (59.2 mg, 0.156 mmol), HOBT (21 mg, 0.156 mmol) and DIPEA (27 μl, 0.156 mmol) in DMF (2 ml) were stirred at room temperature for 18 h. The reaction was diluted with ethyl acetate (150 ml), washed with water (2×30 ml) and dried (magnesium sulphate). The solvent was evaporated under vacuum and the residue chromatographed on a silica flash column eluting with DCM/methanol/triethylamine (96:2:2). Concentration of the product fractions under vacuum N-(6-methyl-4′-{[2-(4-methylpiperazin-1-ylmethyl)anilino]carbonyl}-1,1′-biphenyl-3-yl)-3-furamide (63 mg, 79%). NMR; δH [2H6]-DMSO includes 11.56,(1H, s), 9.94,(1H, s), 8.36–8.34,(2H, m), 8.02,(2H, d), 7.78,(1H, t), 7.68,(1H, d), 7.54,(2H, d), 7.35–7.25,(3H, m), 7.06,(1H, m), 6.98,(1H, m), 3.73,(2H, s), 2.22,(3H, s), 2.11,(3H, s). LCMS: retention time 2.60 min, MH+509.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07151118B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-3fa87cb67c8443139e2ea4c7fb9da8bf
출처 메모uspto-grants-2006_12