4-Fluorobenzonitrile → HCID 23725385, compound

HRID 2219354Notes

Reaction equation

HRID 2219354 reaction equation
[CH2:1]([O:8][CH2:9][C:10]1[NH:11][CH:12]=[C:13]([C:15]2[C:16]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[N:17][O:18][C:19]=2[CH3:20])[N:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.F[C:28]1[CH:35]=[CH:34][C:31]([C:32]#[N:33])=[CH:30][CH:29]=1>>[CH2:1]([O:8][CH2:9][C:10]1[N:11]([C:28]2[CH:35]=[CH:34][C:31]([C:32]#[N:33])=[CH:30][CH:29]=2)[CH:12]=[C:13]([C:15]2[C:16]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[N:17][O:18][C:19]=2[CH3:20])[N:14]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 145174-FluorobenzonitrileHCID 178434979HCID 178434979, compound

Product 1

HCID 23725385HCID 23725385, compoundYield 82%

Procedure

As described for Example 63, 4-(2-benzyloxymethyl-1H-imidazol-4-yl)-5-methyl-3-phenyl-isoxazole (100 mg, 0.29 mmol) using 4-fluorobenzonitrile instead of 4-fluoroacetophenone was converted to the title compound (106 mg, 82%) which was obtained as a white foam. MS: m/e=447.4 [M+H]+.

Sources & evidence

ORD record
ord-a5c4036aace544a19c70caac41eacf0c
Source dataset
uspto-grants-2008_08
Patent number
US07414061B2

Reaction notes

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