3-Fluoro-4-(2-methyl-imidazol-1-yl)-benzoic acid → HCID 68351913, compound

HRID 68894Notes

Reaction equation

HRID 68894 reaction equation
[CH:1]1([NH:4][CH:5]2[CH2:10][CH2:9][N:8]([C:11]3[O:15][N:14]=[C:13]([CH:16]([CH3:18])[CH3:17])[N:12]=3)[CH2:7][CH2:6]2)[CH2:3][CH2:2]1.[F:19][C:20]1[CH:21]=[C:22]([CH:26]=[CH:27][C:28]=1[N:29]1[CH:33]=[CH:32][N:31]=[C:30]1[CH3:34])[C:23](O)=[O:24]>>[CH:1]1([N:4]([CH:5]2[CH2:10][CH2:9][N:8]([C:11]3[O:15][N:14]=[C:13]([CH:16]([CH3:18])[CH3:17])[N:12]=3)[CH2:7][CH2:6]2)[C:23](=[O:24])[C:22]2[CH:26]=[CH:27][C:28]([N:29]3[CH:33]=[CH:32][N:31]=[C:30]3[CH3:34])=[C:20]([F:19])[CH:21]=2)[CH2:2][CH2:3]1

Participants

3

Reactant 2

HCID 286046533-Fluoro-4-(2-methyl-imidazol-1-yl)-benzoic acidHCID 68290028N-cyclopropyl-1-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidin-4-amine

Product 1

HCID 68351913HCID 68351913, compound

Procedure

The title compound is prepared from cyclopropyl-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-piperidin-4-yl]-amine and 3-fluoro-4-(2-methyl-imidazol-1-yl)-benzoic acid following a procedure analogous to that described in Example 90. LC (method 19): tR=3.98 min; Mass spectrum (ESI+): m/z=453 [M+H]+.

Sources & evidence

ORD record
ord-72bf8fa209db465485446497eb778fe7
Source dataset
uspto-grants-2014_09
Patent number
US08822471B2

Reaction notes

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