3-Bromo-5-fluorobenzonitrile → HCID 11552950, compound

HRID 2219539Notes

Reaction equation

HRID 2219539 reaction equation
[CH3:1][O:2][CH2:3][CH2:4][N:5]1[CH:9]=[CH:8][C:7]([NH:10][C:11]([C:13]2[C:18]([NH2:19])=[CH:17][CH:16]=[C:15]([CH3:20])[N:14]=2)=[O:12])=[N:6]1.Br[C:22]1[CH:23]=[C:24]([CH:27]=[C:28]([F:30])[CH:29]=1)[C:25]#[N:26]>>[CH3:1][O:2][CH2:3][CH2:4][N:5]1[CH:9]=[CH:8][C:7]([NH:10][C:11]([C:13]2[C:18]([NH:19][C:22]3[CH:29]=[C:28]([F:30])[CH:27]=[C:24]([C:25]#[N:26])[CH:23]=3)=[CH:17][CH:16]=[C:15]([CH3:20])[N:14]=2)=[O:12])=[N:6]1

Participants

3

Reactant 2

HCID 27833303-Bromo-5-fluorobenzonitrileHCID 86607587HCID 86607587, compound

Product 1

HCID 11552950HCID 11552950, compound

Procedure

The title compound, was prepared from 3-Amino-6-methyl-pyridine-2-carboxylic acid [1-(2-methoxy-ethyl)-1H-pyrazol-3-yl]-amide in accordance with the general method of example, step using 3-Bromo-5-fluorobenzonitrile instead of 3-bromopyridineto yield the final compound as a light yellow solid, MS (ISP): m/e=395.1 (M+H+).

Sources & evidence

ORD record
ord-b638ae9fdde141168dbb505973aac5e2
Source dataset
uspto-grants-2008_08
Patent number
US07414060B2

Reaction notes

Loading…