2-Bromo-4-methylpyridine → HCID 11119933, compound

HRID 730043Notes

Reaction equation

HRID 730043 reaction equation
[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]=1.ClC1C=C(C[C:17]([C:19]2[CH:24]=[CH:23][C:22]([F:25])=[CH:21][CH:20]=2)=[O:18])C=CN=1>>[Br:1][C:2]1[CH:7]=[C:6]([CH2:8][C:17]([C:19]2[CH:24]=[CH:23][C:22]([F:25])=[CH:21][CH:20]=2)=[O:18])[CH:5]=[CH:4][N:3]=1

Participants

3

Reactant 2

HCID 27340872-Bromo-4-methylpyridineHCID 108578732-(2-Chloropyridin-4-yl)-1-(4-fluorophenyl)ethanone

Product 1

HCID 11119933HCID 11119933, compound

Procedure

21c was prepared from 2-bromo-4-methylpyridine (9.6 g; 56 mmol) using the method described in the synthesis of 21a.

Sources & evidence

ORD record
ord-250a344887e14724a7882ae80853825a
Source dataset
uspto-grants-2009_09
Patent number
US07582660B2

Reaction notes

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