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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 480538생성일: 2026년 10월 26일

Dimethylformamide → 6,9-Bis(carboxymethyl)-3-(2,14-dioxo-18,21,24,27,30,33,36-heptaoxa-3,15-diazaheptatriacontanyl)-11,23-dioxo-27,30,33,36,39,42,45-heptaoxa-3,6,9,12,24-pentaazahexatetracontanoic acid

https://huagongshe.com/reaction/480538

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물DTPA dianhydrideHCID 100825—
반응물11-Amino-n-(3,6,9,12,15,18,21-heptaoxadocosyl) undecan-amideHCID 18764642—
생성물6,9-Bis(carboxymethyl)-3-(2,14-dioxo-18,21,24,27,30,33,36-heptaoxa-3,15-diazaheptatriacontanyl)-11,23-dioxo-27,30,33,36,39,42,45-heptaoxa-3,6,9,12,24-pentaazahexatetracontanoic acidHCID 994203774%

반응 단계

N,N-Bis[2-(2,6-dioxo-4-morpholinyl)ethyl]glycine (3.8 g; 10.6 mmol) (commercial product) was added to a suspension of 11-amino-N-(3,6,9,12,15,18,21-heptaoxadocosyl) undecan-amide (11.1 g; 21.1 mmol) in DMF (200 mL). After 15 min the reaction mixture became clear and the conversion was complete. The solvent was evaporated under reduced pressure, the residue was dissolved in CHCl3 and washed with H2O. The organic phase was separated, dried over Na2 SO4 and then evaporated under reduced pressure. The solid was dissolved in H2O and loaded onto an Amberlite® XAD-7 HP resin column (700 mL) and eluted with a CH3CN/H2O gradient. The fraction containing the product was evaporated to give the desired compound (11 g; 7.8 mmol). Yield 74%. HPLC: 85% (area %); K.F. 0.49%. Weight loss (120° C.): 0.45%. The 13C-NMR, MS and IR spectra were consistent with the structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06652834B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-3542142266064229b09d0bd6d40ecd00
출처 메모uspto-grants-2003_11