Reaktion #322200

ord-4c1d530a325b4ddca3b84db636ee8396

Reaktionsgleichung

COCc1nc(N)nc(N)c1-c1cc(Cl)cc(Cl)c1Cl
compound
COCc1nc(N)nc(N)c1-c1cc(Cl)cc(Cl)c1Cl
2,4-Diamino-5-(2,3,5-trichlorophenyl)-6-methoxymethylpyrimidine
N#CCc1c(Cl)cccc1Cl
2,6-dichlorophenylacetonitrile
→
COCc1nc(N)nc(N)c1-c1c(Cl)cccc1Cl
2,4-Diamino-5-(2,6-dichlorophenyl)-6-methoxymethyl-pyrimidine

Edukte

COCc1nc(N)nc(N)c1-c1cc(Cl)cc(Cl)c1Cl
compound
COCc1nc(N)nc(N)c1-c1cc(Cl)cc(Cl)c1Cl
2,4-Diamino-5-(2,3,5-trichlorophenyl)-6-methoxymethylpyrimidine
N#CCc1c(Cl)cccc1Cl
2,6-dichlorophenylacetonitrile

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

This compound was prepared in an analogous manner to the compound of Example 2 from 2,6-dichlorophenylacetonitrile (Aldrich), 204°-207° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05597828uspto-grants-1997_01