Pyridine → HCID 10203446, compound

HRID 672950Notes

Reaction equation

HRID 672950 reaction equation
[CH3:12][O:13][c:14]1[cH:15][cH:16][c:17](-[n:20]2[n:21][c:22]([C:43](=[O:44])[NH2:45])[c:23]3[c:24]2[C:25](=[O:42])[N:26]([c:29]2[cH:30][cH:31][c:32](-[n:35]4[c:36](=[O:41])[cH:37][cH:38][cH:39][cH:40]4)[cH:33][cH:34]2)[CH2:27][CH2:28]3)[cH:18][cH:19]1.[CH3:1][N:2]([CH3:3])[CH:4]=[O:5].[CH3:52][C:53]#[N:54].[Cl:6][C:7]([C:8]([Cl:9])=[O:10])=[O:11].[cH:46]1[cH:47][cH:48][n:49][cH:50][cH:51]1>>[CH3:12][O:13][c:14]1[cH:15][cH:16][c:17](-[n:20]2[n:21][c:22]([C:43]#[N:45])[c:23]3[c:24]2[C:25](=[O:42])[N:26]([c:29]2[cH:30][cH:31][c:32](-[n:35]4[c:36](=[O:41])[cH:37][cH:38][cH:39][cH:40]4)[cH:33][cH:34]2)[CH2:27][CH2:28]3)[cH:18][cH:19]1

Participants

6

Reactant 5

HCID 1049PyridineHCID 6228DimethylformamideHCID 6342AcetonitrileHCID 65578Oxalyl chlorideHCID 10226178HCID 10226178, compound

Product 1

HCID 10203446HCID 10203446, compound

Sources & evidence

ORD record
ord-ac51ae3da10b4d488d7cd3187269d3fa
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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