Ammonium → 2-Trimethylsilylethyl 2-[(4-amino-2-phenylbenzoyl)amino]-4-methylsulfanylbutanoate

HRID 1553788Notes

Reaction equation

HRID 1553788 reaction equation
[CH3:1][Si:2]([CH2:3][CH2:4][O:5][C:6]([CH:7]([NH:8][C:9]([c:10]1[c:11](-[c:19]2[cH:20][cH:21][cH:22][cH:23][cH:24]2)[cH:12][c:13]([N+:16]([O-:17])=[O:18])[cH:14][cH:15]1)=[O:25])[CH2:26][CH2:27][S:28][CH3:29])=[O:30])([CH3:31])[CH3:32].[CH3:37][OH:38].[CH:33]([O-:34])=[O:35].[NH4+:36].[Pd:39]>>[CH3:1][Si:2]([CH2:3][CH2:4][O:5][C:6]([CH:7]([NH:8][C:9]([c:10]1[c:11](-[c:19]2[cH:20][cH:21][cH:22][cH:23][cH:24]2)[cH:12][c:13]([NH2:16])[cH:14][cH:15]1)=[O:25])[CH2:26][CH2:27][S:28][CH3:29])=[O:30])([CH3:31])[CH3:32]

Participants

6

Reactant 5

HCID 223AmmoniumHCID 283FormateHCID 887MethanolHCID 23938PalladiumHCID 234365142-Trimethylsilylethyl 4-methylsulfanyl-2-[(4-nitro-2-phenylbenzoyl)amino]butanoate

Product 1

HCID 234363462-Trimethylsilylethyl 2-[(4-amino-2-phenylbenzoyl)amino]-4-methylsulfanylbutanoate

Sources & evidence

ORD record
ord-d88dfb782da144ef89507862bf12bb9a
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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