HCID 23003365, compound → HCID 23003447, compound

HRID 396498Notes

Reaction equation

HRID 396498 reaction equation
[C:1]([C:4]1[C:9]([Cl:10])=[C:8]([CH2:11][CH3:12])[CH:7]=[CH:6][N:5]=1)(=[O:3])[CH3:2].[BrH:13].[Br:14]C1C=C(C)C=CN=1>>[BrH:14].[Br:13][CH2:2][C:1]([C:4]1[C:9]([Cl:10])=[C:8]([CH2:11][CH3:12])[CH:7]=[CH:6][N:5]=1)=[O:3]

Participants

3

Reactant 2

HCID 23003365HCID 23003365, compoundHCID 23003543HCID 23003543, compound

Product 1

HCID 23003447HCID 23003447, compound

Procedure

The title compound was prepared from 2-acetyl-3-chloro-4-ethylpyridine according to the procedure for preparing 2-bromo-4-methylpyridine hydrobromide described in step 2 of Example 31.

Sources & evidence

ORD record
ord-52f734b4c88f449c8b321ab4e924cf7b
Source dataset
uspto-grants-2003_08
Patent number
US06608070B1

Reaction notes

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