2-Bromo-1-(2-pyridinyl)-1-ethanone hydrobromide → HCID 23003598, compound

HRID 396439

Reaction equation

HRID 396439 reaction equation
[Cl:1][C:2]1[CH:13]=[CH:12][C:5](/[CH:6]=[CH:7]/[C:8]([O:10]C)=[O:9])=[C:4]([NH:14][C:15](OCC)=O)[CH:3]=1.Br.BrC[C:23]([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][N:26]=1)=[O:24]>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:5]([C:6]([CH2:7][C:8]([OH:10])=[O:9])=[C:15]([C:23]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][N:26]=3)=[O:24])[NH:14]2)=[CH:12][CH:13]=1

Participants

3

Reactant 2

HCID 27762312-Bromo-1-(2-pyridinyl)-1-ethanone hydrobromideHCID 23003310Methyl trans-4-chloro-2-(ethoxycarbonylamino)cinnamate

Product 1

HCID 23003598HCID 23003598, compound

Procedure

The title compound were prepared according the procedure described in step 2 of Example 31 from methyl trans-4-chloro-2-(ethoxycarbonylamino)cinnamate (Example 31, step 1) and 2-bromoacetylpyridine hydrobromide (H. McKennis et al., J. Org. Chem., 1963, 387.).

Sources & evidence

ORD record
ord-11bfe3869a1041e7b72e6a159eb972d1
Source dataset
uspto-grants-2003_08
Patent number
US06608070B1

Linked notes

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