Imidazole → 4-(4-Chloro-phenyl)-2-imidazol-1-yl-6-trifluoromethyl-pyrimidine

HRID 1989268Notes

Reaction equation

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

Participants

Reactant 2

HCID 795Imidazole

HCID 4504275HCID 4504275, compound

Product 1

HCID 34150954-(4-Chloro-phenyl)-2-imidazol-1-yl-6-trifluoromethyl-pyrimidine

Procedure

The title compound was prepared from 2-chloro-4-(4-chloro-phenyl)-6-trifluoromethyl-pyrimidine (example A.1) (0.15 g, 0.5 mmol) and commercially available imidazole (0.034 g, 0.5 mmol) according to the general procedure IVa. Obtained as an off-white solid (0.063 g, 39%). MS (EI) 324.1 [(M)+]; mp 175° C.

Sources & evidence

ORD record: ord-49320ac9bc3345ec9e2fc1b59f68b0b7
Source dataset: uspto-grants-2010_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07642264B2

Reaction notes

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