Реакция #322200

ord-4c1d530a325b4ddca3b84db636ee8396

Уравнение реакции

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

Реактанты

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

Реагенты

Нет

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

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

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05597828uspto-grants-1997_01