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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1281733생성일: 2026년 10월 26일

Dichloromethane → N-{3-[3-(4-methylpiperazin-1-ylmethyl)benzamido]-4-methylphenyl}dibenzofuran-4-carboxamide

https://huagongshe.com/reaction/1281733

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물DiisopropylethylamineHCID 81531—
반응물8-Oxatricyclo(7.4.0.0,2,7)trideca-1(9),2(7),3,5,10,12-hexaene-6-carboxylic acidHCID 302872—
반응물N-(5-amino-2-ethylphenyl)-3-(4-methylpiperazin-1-ylmethyl)benzamideHCID 18422068—
용매AcetoneHCID 180—
생성물N-{3-[3-(4-methylpiperazin-1-ylmethyl)benzamido]-4-methylphenyl}dibenzofuran-4-carboxamideHCID 993689654.3%

반응 단계

Diisopropylethylamine (0.4 ml) was added to a stirred mixture of N-(5-amino-2-ethylphenyl)-3-(4-methylpiperazin-1-ylmethyl)benzamide (0.2 g), dibenzofuran-4-carboxylic acid (0.133 g), 2-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate(V) (0.22 g) and methylene chloride (10 ml) and the mixture was stirred at ambient temperature for 16 hours. The mixture was evaporated and the residue was partitioned between methylene chloride and a saturated aqueous sodium bicarbonate solution. The organic phase was dried over magnesium sulphate and evaporated. The residue was purified by column chromatography on silica using increasingly polar mixtures of methylene chloride and methanol as eluent. The material so obtained was dissolved in acetone and reprecipitated by the addition of isohexane. There was thus obtained the title compound (0.164 g); NMR Spectrum: (DMSOd6) 1.15 (t, 3H), 2.25 (s, 3H), 2.35-2.5 (m, 8H), 2.6 (m, 2H), 3.55 (s, 2H), 7.3 (d, 1H), 7.4-7.6 (m, 5H), 7.65 (m, 1H), 7.8-7.9 (m, 5H), 8.2 (d, 1H), 8.35 (d, 1H), 9.95 (s, 1H), 10.43 (s, 1H); Mass Spectrum: M+H+ 547.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06455520B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-e81edc5f94a94a6eb4cfa8814e3d5d85
출처 메모uspto-grants-2002_09