Pyridine → HCID 66719423, compound

HRID 1559109Notes

Reaction equation

HRID 1559109 reaction equation
[CH3:1][O:2][C:3]([CH:4]([CH2:5][c:6]1[cH:7][c:8]2[c:9]([cH:21][cH:22]1)[O:10][CH:11]([c:14]1[cH:15][cH:16][c:17]([OH:20])[cH:18][cH:19]1)[CH2:12][O:13]2)[NH:23][C:24](=[O:25])[O:26][C:27]([CH3:28])([CH3:29])[CH3:30])=[O:31].[CH3:38][C:39](=[O:40])[O:41][C:42](=[O:43])[CH3:44].[Cl:45][CH2:46][Cl:47].[cH:32]1[cH:33][cH:34][n:35][cH:36][cH:37]1>>[CH3:1][O:2][C:3]([CH:4]([CH2:5][c:6]1[cH:7][c:8]2[c:9]([cH:21][cH:22]1)[O:10][CH:11]([c:14]1[cH:15][cH:16][c:17]([O:20][C:39]([CH3:38])=[O:40])[cH:18][cH:19]1)[CH2:12][O:13]2)[NH:23][C:24](=[O:25])[O:26][C:27]([CH3:28])([CH3:29])[CH3:30])=[O:31]

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 7918Acetic AnhydrideHCID 66719235HCID 66719235, compound

Product 1

HCID 66719423HCID 66719423, compound

Sources & evidence

ORD record
ord-dc4615c1184144b484bea7bb707b0cc8
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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