3-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride) → 2-Chloro-4-[1-(3-chloro-4-fluoro-phenyl)-2-methyl-1H-imidazol-4-ylethynyl]-pyridine

HRID 447197Notes

Reaction equation

HRID 447197 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]#[C:9][C:10]2[N:11]=[C:12]([CH3:15])[NH:13][CH:14]=2)[CH:5]=[CH:4][N:3]=1.[Cl:16][C:17]1[CH:18]=[C:19](B(O)O)[CH:20]=[CH:21][C:22]=1[F:23]>>[Cl:1][C:2]1[CH:7]=[C:6]([C:8]#[C:9][C:10]2[N:11]=[C:12]([CH3:15])[N:13]([C:19]3[CH:20]=[CH:21][C:22]([F:23])=[C:17]([Cl:16])[CH:18]=3)[CH:14]=2)[CH:5]=[CH:4][N:3]=1

Participants

3

Procedure

The title compound, MS: m/e=347.2 (M+H+), was prepared in accordance with the general method of example 7 from 2-chloro-4-(2-methyl-1H-imidazol-4-ylethynyl)-pyridine and 3-chloro-4-fluoro-benzene boronic acid.

Sources & evidence

ORD record
ord-d759feb5228f4b228f1edcfe38a6c789
Source dataset
uspto-grants-2013_07
Patent number
US08481548B2

Reaction notes

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