Hydrazine → [5-(5-isopropyl-2,4-dimethoxy-phenyl)-4-(1-methyl-1H-indol-5-yl)-4H-[1,2,4]triazol-3-yl]-phenylamine

HRID 555946

Reaktionsgleichung

Reaktionsgleichung von HRID 555946
[CH:1]([C:4]1[C:5]([O:25][CH3:26])=[CH:6][C:7]([O:23][CH3:24])=[C:8]([CH:22]=1)[C:9]([NH:11][C:12]1[CH:13]=[C:14]2[C:18](=[CH:19][CH:20]=1)[N:17]([CH3:21])[CH:16]=[CH:15]2)=S)([CH3:3])[CH3:2].[NH2:27][NH2:28].C(N(C(C)C)CC)(C)C.[CH:38]1[CH:43]=[CH:42][C:41]([N:44]=[C:45](Cl)Cl)=[CH:40][CH:39]=1>O1CCOCC1>[CH:1]([C:4]1[C:5]([O:25][CH3:26])=[CH:6][C:7]([O:23][CH3:24])=[C:8]([C:9]2[N:11]([C:12]3[CH:13]=[C:14]4[C:18](=[CH:19][CH:20]=3)[N:17]([CH3:21])[CH:16]=[CH:15]4)[C:45]([NH:44][C:41]3[CH:42]=[CH:43][CH:38]=[CH:39][CH:40]=3)=[N:27][N:28]=2)[CH:22]=1)([CH3:3])[CH3:2]

Komponenten

6

Edukt 4

HCID 9321HydrazineHCID 12145Phenylimidocarbonyl chlorideHCID 81531DiisopropylethylamineHCID 59729557HCID 59729557, Verbindung

Produkt 1

HCID 59729571[5-(5-isopropyl-2,4-dimethoxy-phenyl)-4-(1-methyl-1H-indol-5-yl)-4H-[1,2,4]triazol-3-yl]-phenylamine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A flask was charged with 5-isopropyl-2,4-dimethoxy-N-(1-methyl-1H-indol-5-yl)-thiobenzamide (123 mg; 0.33 mmol), dioxane (2 mL), and hydrazine (0.5 mL). The reaction was heated to 100° C. for one hour, and the solvent was removed by evaporation. To the solid cake was added ethyl acetate (10 mL) and 10% aqueous potassium carbonate (1 mL), and it was shaken until the solid was completely dissolved. The organic layer was isolated, and dried with sodium sulfate. To the crude intermediate in the organic layer was added diisopropylethylamine (86 mg, 0.66 mmol) and phenylisocyanide dichloride (88 mg; 1.5 eq.). The reaction was stirred overnight, and washed with saturated aqueous ammonium chloride, dried with sodium sulfate, and the product was purified by column chromatography to give [5-(5-Isopropyl-2,4-dimethoxy-phenyl)-4-(1-methyl-1H-indol-5-yl)-4H-[1,2,4]triazol-3-yl]-phenyl-amine (64 mg).

Aufarbeitung

  1. customthe solvent was removed by evaporation
  2. additionTo the solid cake was added ethyl acetate (10 mL) and 10% aqueous potassium carbonate (1 mL), and it
  3. dissolutionwas completely dissolved
  4. customThe organic layer was isolated
  5. dry with materialdried with sodium sulfate
  6. stirringThe reaction was stirred overnight
  7. washwashed with saturated aqueous ammonium chloride
  8. dry with materialdried with sodium sulfate
  9. customthe product was purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-a105fc2b3ee5488883dcfe83a1d5040a
Quelldatensatz
uspto-grants-2011_11
Patentnummer
US08053456B2

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