Pyridine → HCID 22291038, compound

HRID 1138342Notes

Reaction equation

HRID 1138342 reaction equation
[CH2:42]([Cl:43])[Cl:44].[CH3:1][S:2]([Cl:3])(=[O:4])=[O:5].[NH2:6][c:7]1[cH:8][c:9]([C:10](=[O:11])[NH:12][c:13]2[cH:14][cH:15][c:16]([CH3:32])[c:17]([NH:19][C:20]([c:21]3[cH:22][c:23]([O:29][CH3:30])[c:24]([O:27][CH3:28])[cH:25][cH:26]3)=[O:31])[cH:18]2)[cH:33][cH:34][cH:35]1.[cH:36]1[cH:37][cH:38][n:39][cH:40][cH:41]1>>[CH3:1][S:2](=[O:4])(=[O:5])[NH:6][c:7]1[cH:8][c:9]([C:10](=[O:11])[NH:12][c:13]2[cH:14][cH:15][c:16]([CH3:32])[c:17]([NH:19][C:20]([c:21]3[cH:22][c:23]([O:29][CH3:30])[c:24]([O:27][CH3:28])[cH:25][cH:26]3)=[O:31])[cH:18]2)[cH:33][cH:34][cH:35]1

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 31297Methanesulfonyl chlorideHCID 22291106HCID 22291106, compound

Product 1

HCID 22291038HCID 22291038, compound

Sources & evidence

ORD record
ord-4f8d7ca785654b5a92cde04dd00e7c14
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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