3-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride) → HCID 23725268, compound

HRID 2219323Notes

Reaction equation

HRID 2219323 reaction equation
[NH:1]1[CH:5]=[C:4]([C:6]2[C:7]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[N:8][O:9][C:10]=2[CH3:11])[N:3]=[CH:2]1.[Cl:18][C:19]1[CH:20]=[C:21](B(O)O)[CH:22]=[CH:23][C:24]=1[F:25]>>[Cl:18][C:19]1[CH:20]=[C:21]([N:1]2[CH:5]=[C:4]([C:6]3[C:7]([C:12]4[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=4)=[N:8][O:9][C:10]=3[CH3:11])[N:3]=[CH:2]2)[CH:22]=[CH:23][C:24]=1[F:25]

Participants

3

Reactant 2

HCID 27346603-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride)HCID 178434980HCID 178434980, compound

Product 1

HCID 23725268HCID 23725268, compoundYield 5%

Procedure

As described for Example 3, 4-(1H-imidazol-4-yl)-5-methyl-3-phenyl-isoxazole (112.6 mg, 0.5 mmol) was converted, using 3-chloro-4-fluorophenylboronic acid instead of 4-fluorophenylboronic acid, to the title compound (8 mg, 5%) which was obtained as a white solid. MS (ESI): m/e=353.9 [M+H]+.

Sources & evidence

ORD record
ord-29395579dee34daaae894c9be5e16755
Source dataset
uspto-grants-2008_08
Patent number
US07414061B2

Reaction notes

Loading…