Ammonia → 2-Pentylthiazolo[4,5-c]quinolin-4-amine

HRID 430542노트

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HRID 430542 반응식
[CH2:1]([C:6]1[S:7][C:8]2[C:17]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[N:11]=[C:10]([NH:18]C(=O)C(Cl)(Cl)Cl)[C:9]=2[N:25]=1)[CH2:2][CH2:3][CH2:4][CH3:5].N.ClCCl>CO>[CH2:1]([C:6]1[S:7][C:8]2[C:17]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[N:11]=[C:10]([NH2:18])[C:9]=2[N:25]=1)[CH2:2][CH2:3][CH2:4][CH3:5]

참가 물질

5

실험 절차

Trichloroacetyl isocyanate (0.51 mL) was added to a solution of 2-pentylthiazolo[4,5-c]quinoline-5N-oxide (0.78 g) in dichloromethane (50 mL). The reaction mixture was stirred at ambient temperature for about 75 minutes and then concentrated under vacuum to provide crude N-(2-pentylthiazolo[4,5-c]quinolin-4-yl)trichloroacetamide. The amide was combined with a solution of ammonia in methanol (40 ml of 2M). Dichloromethane was added to bring all of the material into solution. When the reaction was completed as indicated by thin layer chromatography, the reaction a mixture was concentrated under vacuum. The residue was mixed with dichloromethane and sodium bicarbonate. The organic layer was separated, washed with sodium bicarbonate then with water, dried over magnesium sulfate and then concentrated under vacuum to provide a white solid. This material was recrystallized from ethyl acetate to provide 2-pentylthiazolo[4,5-c]quinolin-4-amine as an off-white crystalline solid, m.p. 119-121° C. Analysis: Calculated for C15H17N3S: % C, 66.39; % H, 6.31; % N, 15.48; Found: % C, 66.21; % H, 6.35; % N, 15.39.

후처리

  1. customthe reaction a mixture
  2. concentrationwas concentrated under vacuum
  3. additionThe residue was mixed with dichloromethane and sodium bicarbonate
  4. customThe organic layer was separated
  5. washwashed with sodium bicarbonate
  6. dry with materialwith water, dried over magnesium sulfate
  7. concentrationconcentrated under vacuum
  8. customto provide a white solid
  9. customThis material was recrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-f3a1b98bc7cd457c9dca07fcdc3a0722
출처 데이터셋
uspto-grants-2001_11
특허 번호
US06323200B1

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