Pyridine → HCID 59129384, compound

HRID 167132Notes

Reaction equation

HRID 167132 reaction equation
[C:26]([CH2:27][CH2:28][CH3:29])(=[O:30])[Cl:31].[Cl:32][CH2:33][Cl:34].[NH2:1][c:2]1[c:3]([C:11]#[C:12][C:13]([C:14](=[O:15])[O:16][CH3:17])([CH3:18])[CH3:19])[cH:4][c:5]([N+:8](=[O:9])[O-:10])[cH:6][cH:7]1.[cH:20]1[cH:21][cH:22][n:23][cH:24][cH:25]1>>[NH:1]([c:2]1[c:3]([C:11]#[C:12][C:13]([C:14](=[O:15])[O:16][CH3:17])([CH3:18])[CH3:19])[cH:4][c:5]([N+:8](=[O:9])[O-:10])[cH:6][cH:7]1)[C:26]([CH2:27][CH2:28][CH3:29])=[O:30]

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 8855Butyryl chlorideHCID 59129298Methyl 4-(2-amino-5-nitrophenyl)-2,2-dimethylbut-3-ynoate

Product 1

HCID 59129384HCID 59129384, compound

Sources & evidence

ORD record
ord-a79e8a68a5964fd690df493884ab3b69
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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