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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 480541생성일: 2026년 10월 25일

Triethylamine → 6,9-Bis(carboxymethyl)-11,19-dioxo-3-[2-[[2-[2-[(1-oxooctadecyl)oxy]ethoxy]ethyl]amino]-2-oxoethyl]-15,18-dioxa-3,6,9,12-tetraaza-hexatriacontanoic Acid

https://huagongshe.com/reaction/480541

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DTPA dianhydrideHCID 100825—
반응물Octadecanoic acid 2-(2-aminoethoxy)ethyl ester hydrochlorideHCID 85772808—
용매DimethylformamideHCID 6228—
생성물6,9-Bis(carboxymethyl)-11,19-dioxo-3-[2-[[2-[2-[(1-oxooctadecyl)oxy]ethoxy]ethyl]amino]-2-oxoethyl]-15,18-dioxa-3,6,9,12-tetraaza-hexatriacontanoic AcidHCID 981239727.3%

반응 단계

N,N-Bis[2-(2,6-dioxo-4-morpholinyl)ethyl]glycine (1.9 g; 5.5 mmol) (commercial product) was added to a solution of octadecanoic acid 2-(2-aminoethoxy)ethyl ester hydrochloride (4.5 g; 11 mmol) and Et3N (1.5 g; 14 mmol) in DMF (150 mL) at 60° C. After 5 min the temperature was decreased to 45° C. After 2.5 h the mixture was cooled to room temperature to give a precipitate that was filtered, washed with acetone/H2O 15/5, then with acetone. The crude was dissolved in acetone and 0.1 N HCl and the solution heated at 50° C. After 10 min the solution was cooled to room temperature to afford a precipitate which was filtered, washed with acetone/H2O 15/5 then with acetone and dried under reduced pressure to give the desired compound (1.7 g; 1.5 mmol). Yield 27%. HPLC: 100% (area %). HPCE: 100% (area). K.F.: 3.11%. Weight loss (120° C.): 4.49%. The 1H-NMR, 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-b6848dee211143ea92c74016e72068a6
출처 메모uspto-grants-2003_11