Acrolein dimer → [(1-Cyclopentyl-1H-tetrazol-5-yl)-(3,4-dihydro-2H-pyran-2-yl)-methyl]-(3-imidazol-1-yl-propyl)-amine

HRID 18464

Reaktionsgleichung

Reaktionsgleichung von HRID 18464
[N:1]1([CH2:6][CH2:7][CH2:8][NH2:9])[CH:5]=[CH:4][N:3]=[CH:2]1.[O:10]1[CH:15]=[CH:14][CH2:13][CH2:12][CH:11]1[CH:16]=O.C[Si]([N:22]=[N+:23]=[N-:24])(C)C.[N+:25]([CH:27]1[CH2:31][CH2:30][CH2:29][CH2:28]1)#[C-:26]>CO>[CH:27]1([N:25]2[C:26]([CH:16]([NH:9][CH2:8][CH2:7][CH2:6][N:1]3[CH:5]=[CH:4][N:3]=[CH:2]3)[CH:11]3[CH2:12][CH2:13][CH:14]=[CH:15][O:10]3)=[N:24][N:23]=[N:22]2)[CH2:31][CH2:30][CH2:29][CH2:28]1

Komponenten

6

Edukt 4

HCID 60994Acrolein dimerHCID 78378AzidotrimethylsilaneHCID 787361H-Imidazole-1-propanamineHCID 2734784Cyclopentyl Isocyanide

Produkt 1

HCID 25059135[(1-Cyclopentyl-1H-tetrazol-5-yl)-(3,4-dihydro-2H-pyran-2-yl)-methyl]-(3-imidazol-1-yl-propyl)-amine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

3-Imidazol-1-yl-propylamine (1 mmol) and 3,4-Dihydro-2H-pyran-2-carbaldehyde (1 mmol) were combined in methanol (2 ml, dry). After 2 hours Trimethylsilylazide (5 mmol) and Isocyano-cyclopentan (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-3e0f9a51eab2438f8ca1618be1899848
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07741354B2

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