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HRID 1280505作成日:2026年10月25日

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/1280505

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1-(2-aminoethyl)-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-4-amine hydrochlorideHCID 22478988—
反応物N-Hydroxysuccinimido-d-biotinHCID 129676281—
溶媒ChloroformHCID 6212—
生成物n-[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%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06451810B1
出典データセットuspto-grants-2002_09
ORD IDord-6e81519240024cf78f12eddd867e7545
出典メモuspto-grants-2002_09