Acrylonitrile → HCID 54350943, compound

HRID 2125007Notes

Reaction equation

HRID 2125007 reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][CH:11]([C:14](=[O:15])[NH:16][c:17]2[c:18]([C:19](=[O:20])[NH:21][c:22]3[n:23][cH:24][c:25]([Cl:28])[cH:26][cH:27]3)[cH:29][c:30]([I:33])[cH:31][cH:32]2)[CH2:12][CH2:13]1.[CH2:34]=[CH:35][C:36]#[N:37]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][CH:11]([C:14](=[O:15])[NH:16][c:17]2[c:18]([C:19](=[O:20])[NH:21][c:22]3[n:23][cH:24][c:25]([Cl:28])[cH:26][cH:27]3)[cH:29][c:30]([CH:34]=[CH:35][C:36]#[N:37])[cH:31][cH:32]2)[CH2:12][CH2:13]1

Participants

3

Reactant 2

HCID 7855AcrylonitrileHCID 219066352-[(1-tert-butoxycarbonylpiperidin-4-ylcarbonyl)amino]-N-(5-chloropyridin-2-yl)-5-iodobenzamide

Product 1

HCID 54350943HCID 54350943, compound

Sources & evidence

ORD record
ord-3a504bcab804455a8203f4dd72c22cc7
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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