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

HRID 393923Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 393923
[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]

Komponenten

5

Versuchsvorschrift

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 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.

Aufarbeitung

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

Quellen und Nachweise

ORD-Eintrag
ord-3b7dcce0d1784e6ea186e60d3aa68970
Quelldatensatz
uspto-grants-2004_10
Patentnummer
US06809203B2

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