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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 746530생성일: 2026년 10월 25일

Triethylamine → n-[2-(4-Amino-2-(ethoxymethyl)-1h-imidazo[4,5-c]quinolin-1-yl)ethyl]-5-(2-oxoperhydrothieno[3,4-d]imidazol-4-yl)pentanamide

https://huagongshe.com/reaction/746530

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-(2-aminoethyl)-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-4-amine hydrochlorideHCID 22478988—
반응물N-Hydroxysuccinimido-d-biotinHCID 129676281—
용매ChloroformHCID 6212—
생성물n-[2-(4-Amino-2-(ethoxymethyl)-1h-imidazo[4,5-c]quinolin-1-yl)ethyl]-5-(2-oxoperhydrothieno[3,4-d]imidazol-4-yl)pentanamideHCID 2351269013.3%

반응 단계

Triethylamine (1.2 g, 11.4 mmol) was added in a single portion to a slurry of 1-(2-aminoethyl)-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-4-amine hydrochloride (3.39 g, 10.53 mmol) in chloroform (150 mL). The reaction mixture became clear. N-hydroxysuccinimidobiotin (3.0 g, 8.79 mmol) was then slowly added. After 2 hours the turbid reaction mixture was heated to reflux. The reaction mixture was maintained at reflux overnight and became clear. The reaction mixture was allowed to cool to ambient temperature and then it was quenched with water. The layers were separated. The organic layer was dried over magnesium sulfate and then concentrated to provide an off-white solid. This material was recrystallized from 8:2 ethanol:water to provide a white solid. A portion of this material was purified by prep HPLC eluting with water/acetonitrile/trifluoroacetic acid to provide 0.6 g of N1-[2-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]-5-(2-oxoperhydrothieno[3,4-d]imidazol-4-yl)pentanamide as the ditrifluoroacetate salt, m.p. 171-175° C. Analysis: Calculated for: C25H33N7O3S.2 C2HF3O2: % C, 47.09; % H, 4.77; % N, 13.26; Found: % C, 47.06; % H, 5.17; % N, 13.31.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07393859B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-0fc4d6308eb9463f83e668f0e731a161
출처 메모uspto-grants-2008_07