Reaktion #4943

ord-6d86f383aca44f438845b19594bf30af

Reaktionsgleichung

CN1CC(CCCl)Oc2ncccc2C1=S
2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f]-1,4-oxazepine-5(4H)-thione
[H-].[Na+]
sodium hydride
c1cn[nH]c1
pyrazole
[H][H]
hydrogen
CN1CC(CCn2cccn2)Oc2ncccc2C1=S
2,3-Dihydro-4-methyl-2-[2-(1H-pyrazol-1-yl)ethyl]pyrido[3,2-f][1,4]oxazepine-5(4H)-thione

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction flask was sealed

Vorschrift

To a suspension of 2.16 g (0.054 mole) of sodium hydride in 20 ml of dimethylformamide was added dropwise a solution of 2.92 g (0.043 mole) of pyrazole in 10 ml of dimethylformamide. There was a slight exotherm at this point with some evolution of hydrogen gas. The resulting solution was then added dropwise to a solution of 10.0 g (0.039 mole) of 2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f]-1,4-oxazepine-5(4H)-thione in 30 ml of dimethylformamide. The reaction flask was sealed and stirred overnight at room temperature.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04727152uspto-grants-1988_02