Reaktion #7010

ord-f6db3128a3104baab6ac26020f6aaa80

Reaktionsgleichung

Cc1nnc(C2CCN(C(=O)OC(C)(C)C)CC2)o1
4-(5-Methyl-[1,3,4]oxadiazol-2-yl)-piperidine-1-carboxylic acid tert-butyl ester
NCc1ccccc1
benzylamine
NCc1ccccc1
benzylamine
Cc1nnc(C2CCN(C(=O)OC(C)(C)C)CC2)n1Cc1ccccc1
title compound
Ausbeute 70.4%
Cc1nnc(C2CCN(C(=O)OC(C)(C)C)CC2)n1Cc1ccccc1
4-(4-Benzyl-5-methyl-4H-[1,2,4]triazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester
Ausbeute 70.4%

Reaktionsbedingungen

Temperatur
150°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was cooled to room temperature
  2. 2
    Sonstigethe reaction mixture was purified by chromatography on silica gel
  3. 3
    SonstigeThe material isolated
  4. 4
    Sonstigewas triturated with diethyl ether

Vorschrift

4-(5-Methyl-[1,3,4]oxadiazol-2-yl)-piperidine-1-carboxylic acid tert-butyl ester (5 g, 18.7 mmol) (see reference WO 0039125), benzylamine (2.5 ml, 22 mmol) and magnesium chloride (100 mg) were heated at 150° C. for 1 hour, a further quantity of benzylamine (2.5 ml, 22 mmol) was added and the mixture was heated at 150° C. for 4 hours. The reaction mixture was cooled to room temperature and the reaction mixture was purified by chromatography on silica gel using methanol in dichloromethane as eluant (3:97). The material isolated was triturated with diethyl ether to give the title compound as a white solid (4.69 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084145B2uspto-grants-2006_08