Acetate → N-(5-Ethenyl-2-pyridinyl)-2-methylpropanamide

Reaction equation

[C:1]([CH:2]([CH3:3])[CH3:4])(=[O:5])[NH:6][c:7]1[n:8][cH:9][c:10]([Br:13])[cH:11][cH:12]1.[C:23]([O-:24])(=[O:25])[CH3:26].[C:28]([O-:29])(=[O:30])[CH3:31].[CH2:21]=[CH2:22].[CH3:14][CH2:15][N:16]([CH2:17][CH3:18])[CH2:19][CH3:20].[CH3:32][C:33]#[N:34].[Pd+2:27]>>[C:1]([CH:2]([CH3:3])[CH3:4])(=[O:5])[NH:6][c:7]1[n:8][cH:9][c:10]([CH:14]=[CH2:15])[cH:11][cH:12]1

Participants

Reactant 6

HCID 175Acetate2×

HCID 6325Ethylene

HCID 6342Acetonitrile

HCID 8471Triethylamine

HCID 105144Allyl(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)chloropalladium(II)

HCID 14988412N-(5-Bromo-2-pyridinyl)-2-methylpropanamide

Product 1

HCID 14988413N-(5-Ethenyl-2-pyridinyl)-2-methylpropanamide

Sources & evidence

ORD record: ord-f09c3920b9b141bba7ecd775ef5d9aa8
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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