HCID 57468661, compound → HCID 57468771, compound

HRID 1989189Notes

Reaction equation

HRID 1989189 reaction equation
Cl[C:2]1[N:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[C:4]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([F:21])([F:20])[F:19])[CH:13]=2)[N:3]=1.[Br:22][C:23]1[N:24]=[CH:25][NH:26][CH:27]=1>>[Br:22][C:23]1[N:24]=[CH:25][N:26]([C:2]2[N:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[C:4]([C:12]3[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([F:21])([F:20])[F:19])[CH:13]=3)[N:3]=2)[CH:27]=1

Participants

3

Reactant 2

HCID 57468661HCID 57468661, compoundHCID 178418934HCID 178418934, compound

Product 1

HCID 57468771HCID 57468771, compound

Procedure

The title compound was prepared from 2-chloro-4-trifluoromethyl-6-(3-trifluoromethylphenyl)-pyrimidine (example A.42) (0.65 g, 2.0 mmol) and commercially available 4-bromo-imidazole (0.44 g, 3.0 mmol) according to the general procedure IVa. Obtained as a light yellow solid (0.64 g, 73%). MS (ISP) 439.1 [(M+H)+]; mp 158.5° C.

Sources & evidence

ORD record
ord-e9856b53243e4f7986695f72174efa30
Source dataset
uspto-grants-2010_01
Patent number
US07642264B2

Reaction notes

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