Imidazole → HCID 16128673, compound

HRID 2266415Notes

Reaction equation

HRID 2266415 reaction equation
[C:1]1([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:6]=[CH:5][CH:4]=[C:3]([N:7]2[CH:11]=[C:10]([N:12]3[CH:16]=[CH:15]C=N3)[N:9]=[CH:8]2)[CH:2]=1.[NH:23]1C=CN=[CH:24]1>>[C:1]1([C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:6]=[CH:5][CH:4]=[C:3]([N:7]2[CH:11]=[C:10]([N:12]3[CH:16]=[CH:15][N:23]=[CH:24]3)[N:9]=[CH:8]2)[CH:2]=1

Participants

3

Reactant 2

HCID 795ImidazoleHCID 16128672HCID 16128672, compound

Product 1

HCID 16128673HCID 16128673, compoundYield 60%

Procedure

The title compound was prepared by a method analogous to the synthesis of 1-(1-Biphenyl-3-yl-1H-imidazol-4-yl)-1H-pyrazole and using imidazole to give 60% yield. HRMS (ESI+): m/z=286.3366 [M+H]

Workup

  1. customto give 60% yield

Sources & evidence

ORD record
ord-2f21aa6ff04441488141fefaf8fd04ad
Source dataset
uspto-grants-2010_12
Patent number
US07858649B2

Reaction notes

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