Reaktion #1869190

ord-281727cb74e9404f8ec80ef3f0e73d68

Reaktionsgleichung

C=Cc1ccnc2ccc(C#N)cc12
( d )
C=Cc1ccnc2ccc(C#N)cc12
4-Vinyl-quinoline-6-carbonitrile
CC(C)(C)OC(=O)NC1CCNCC1
piperidin-4-yl-carbamic acid tert-butyl ester
CC(C)(C)OC(=O)NC1CCN(CCc2ccnc3ccc(C#N)cc23)CC1
product
Ausbeute 99.9%
CC(C)(C)OC(=O)NC1CCN(CCc2ccnc3ccc(C#N)cc23)CC1
{1-[2-(6-Cyano-quinolin-4-yl)-ethyl]-piperidin-4-yl}-carbamic acid tert-butyl ester
Ausbeute 99.9%

Lösungsmittel

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe product was purified by flash silica chromatography
  2. 2
    Wascheneluting with a 0-2% methanol in chloroform gradient

Vorschrift

A mixture of (d) (150 mg, 0.8 mmol), piperidin-4-yl-carbamic acid tert-butyl ester (166 mg, 0.8 mmol) and chloroform (0.5 ml) were heated at 50° C. in a loosely capped vial for 6 hours. The product was purified by flash silica chromatography eluting with a 0-2% methanol in chloroform gradient affording the product as a foam (304 mg, 96%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07498326B2uspto-grants-2009_03