(2,6-Dichlorophenyl)acetonitrile → 2,4-Diamino-5-(2,6-dichlorophenyl)-6-methoxymethyl-pyrimidine

HRID 235018Notes

Reaction equation

HRID 235018 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([C:9]2[CH:14]=[C:13](Cl)[CH:12]=[C:11](Cl)[C:10]=2[Cl:17])=[C:4]([CH2:18][O:19][CH3:20])[N:3]=1.[Cl:21]C1C=CC=C(Cl)C=1CC#N>>[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([C:9]2[C:14]([Cl:21])=[CH:13][CH:12]=[CH:11][C:10]=2[Cl:17])=[C:4]([CH2:18][O:19][CH3:20])[N:3]=1

Participants

3

Procedure

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

Sources & evidence

ORD record
ord-4c1d530a325b4ddca3b84db636ee8396
Source dataset
uspto-grants-1997_01
Patent number
US05597828

Reaction notes

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