Azidotrimethylsilane → [[1-(4-Chloro-benzyl)-1H-tetrazol-5-yl]-(1H-indol-5-yl)-methyl]-(3-imidazol-1-yl-propyl)-amine

HRID 18463

Reaktionsgleichung

Reaktionsgleichung von HRID 18463
[N:1]1([CH2:6][CH2:7][CH2:8][NH2:9])[CH:5]=[CH:4][N:3]=[CH:2]1.[NH:10]1[C:18]2[C:13](=[CH:14][C:15]([CH:19]=O)=[CH:16][CH:17]=2)[CH:12]=[CH:11]1.C[Si]([N:25]=[N+:26]=[N-:27])(C)C.[Cl:28][C:29]1[CH:34]=[CH:33][C:32]([CH2:35][N+:36]#[C-:37])=[CH:31][CH:30]=1>CO>[Cl:28][C:29]1[CH:34]=[CH:33][C:32]([CH2:35][N:36]2[C:37]([CH:19]([NH:9][CH2:8][CH2:7][CH2:6][N:1]3[CH:5]=[CH:4][N:3]=[CH:2]3)[C:15]3[CH:14]=[C:13]4[C:18](=[CH:17][CH:16]=3)[NH:10][CH:11]=[CH:12]4)=[N:27][N:26]=[N:25]2)=[CH:31][CH:30]=1

Komponenten

6

Versuchsvorschrift

3-Imidazol-1-yl-propylamine (1 mmol) and 1H-Indole-5-carbaldehyde (1 mmol) were combined in methanol (2 ml, dry). After 2 hours Trimethylsilylazide (5 mmol) and 1-Chloro-4-isocyanomethyl-benzene (1 mmol) was added. The reaction was stirred at room temperature for 48 h. After evaporation of the solvent the residue was purified with chromatographic methods.

Aufarbeitung

  1. customAfter evaporation of the solvent the residue
  2. customwas purified with chromatographic methods

Quellen und Nachweise

ORD-Eintrag
ord-f940c1933ff04e1d9ae29bae6ac77221
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07741354B2

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