Pyridine → HCID 21224193, compound

HRID 2344439Notes

Reaction equation

HRID 2344439 reaction equation
[CH2:35]([Cl:36])[Cl:37].[CH3:28][N:29]([S:30](=[O:31])(=[O:32])[Cl:33])[CH3:34].[NH2:1][CH:2]([C:3](=[O:4])[NH:5][O:6][C:7]([CH3:8])([CH3:9])[CH3:10])[CH2:11][S:12](=[O:13])(=[O:14])[c:15]1[cH:16][cH:17][c:18]([O:21][c:22]2[cH:23][cH:24][cH:25][cH:26][cH:27]2)[cH:19][cH:20]1.[cH:38]1[cH:39][cH:40][n:41][cH:42][cH:43]1>>[NH:1]([CH:2]([C:3](=[O:4])[NH:5][O:6][C:7]([CH3:8])([CH3:9])[CH3:10])[CH2:11][S:12](=[O:13])(=[O:14])[c:15]1[cH:16][cH:17][c:18]([O:21][c:22]2[cH:23][cH:24][cH:25][cH:26][cH:27]2)[cH:19][cH:20]1)[S:30]([N:29]([CH3:28])[CH3:34])(=[O:31])=[O:32]

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 83372Dimethylsulphamoyl chlorideHCID 21224131HCID 21224131, compound

Product 1

HCID 21224193HCID 21224193, compound

Sources & evidence

ORD record
ord-92c8b347344d4aee96cb17a659ef51c0
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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