Hydrochloric Acid → 1,4-Dihydro-6,7-dichloro-5-[5-(N,N-dimethylaminomethyl)-1,2,3-benzotriazol-1-ylmethyl]quinoxalin-2,3-dione

HRID 1957115Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1957115
[Cl:1][C:2]1[C:3]([CH2:17][N:18]2[C:22]3[CH:23]=[CH:24][C:25]([CH2:27][N:28]([CH3:30])[CH3:29])=[CH:26][C:21]=3[N:20]=[N:19]2)=[C:4]2[C:9](=[CH:10][C:11]=1[Cl:12])[N:8]=[C:7]([O:13]C)[C:6]([O:15]C)=[N:5]2.Cl>O1CCOCC1>[Cl:1][C:2]1[C:3]([CH2:17][N:18]2[C:22]3[CH:23]=[CH:24][C:25]([CH2:27][N:28]([CH3:30])[CH3:29])=[CH:26][C:21]=3[N:20]=[N:19]2)=[C:4]2[C:9](=[CH:10][C:11]=1[Cl:12])[NH:8][C:7](=[O:13])[C:6](=[O:15])[NH:5]2

Komponenten

4

Versuchsvorschrift

A mixture of 6,7-dichloro-2,3-dimethoxy-5-[5-(N,N-dimethylaminomethyl)-1,2,3-benzotriazol-1-ylmethyl]quinoxaline (Preparation 24, 110 mg, 0.25 mmol), 2M hydrochloric acid (10 mL) and dioxane (10 mL) was heated at reflux for 5.5 hours. The mixture was concentrated under reduced pressure, diluted with acetone (10 mL) and filtered. The solid was dried under vacuum to give the title compound as an off-white solid (97 mg, 94%), mp 282° C. Found: C, 45.57; H, 4.00; N, 17.67. C18H16Cl2N6 O2. HCl.H2O requires C, 45.64; H, 4.04; N, 17.74%.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureat reflux for 5.5 hours
  3. concentrationThe mixture was concentrated under reduced pressure
  4. additiondiluted with acetone (10 mL)
  5. filtrationfiltered
  6. customThe solid was dried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-b0c66b9f8be8405bb337e333ed816dd8
Quelldatensatz
uspto-grants-1998_07
Patentnummer
US05783572

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