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

HRID 353846노트

반응식

HRID 353846 반응식
C(N(CC)CC)C.Cl.[NH2:9][CH2:10][CH2:11][N:12]1[C:24]2[C:23]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[N:17]=[C:16]([NH2:25])[C:15]=2[N:14]=[C:13]1[CH2:26][O:27][CH2:28][CH3:29].O[N:31]1[C:52](=[O:53])[NH:51][C@H:50]2[C@@H:32]1[CH2:33][S:34][C@H:35]2[CH2:36][CH2:37][CH2:38][CH:39](N1C(=O)CCC1=O)[C:40](=O)[OH:41]>C(Cl)(Cl)Cl>[NH2:25][C:16]1[C:15]2[N:14]=[C:13]([CH2:26][O:27][CH2:28][CH3:29])[N:12]([CH2:11][CH2:10][NH:9][C:40](=[O:41])[CH2:39][CH2:38][CH2:37][CH2:36][CH:35]3[CH:50]4[CH:32]([NH:31][C:52](=[O:53])[NH:51]4)[CH2:33][S:34]3)[C:24]=2[C:23]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[N:17]=1

참가 물질

5

실험 절차

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.

후처리

  1. customAfter 2 hours the turbid reaction mixture
  2. temperaturewas heated to reflux
  3. temperatureThe reaction mixture was maintained
  4. temperatureat reflux overnight
  5. customit was quenched with water
  6. customThe layers were separated
  7. dry with materialThe organic layer was dried over magnesium sulfate
  8. concentrationconcentrated
  9. customto provide an off-white solid
  10. customThis material was recrystallized from 8:2 ethanol
  11. customwater to provide a white solid
  12. customA portion of this material was purified by prep HPLC
  13. washeluting with water/acetonitrile/trifluoroacetic acid

출처 및 근거

ORD 기록
ord-e60d1c2158764ec3b9c89e1f1e969b87
출처 데이터셋
uspto-grants-2004_06
특허 번호
US06756382B2

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