Pyridine → HCID 23114764, compound

HRID 2322937Notes

Reaction equation

HRID 2322937 reaction equation
[CH2:6]([Cl:7])[Cl:8].[CH3:1][S:2]([Cl:3])(=[O:4])=[O:5].[CH3:42][CH2:43][O:44][C:45](=[O:46])[CH3:47].[Cl:9][c:10]1[cH:11][cH:12][c:13]([S:16](=[O:17])(=[O:18])[CH:19]([c:20]2[cH:21][c:22]([NH2:27])[n:23][cH:24][c:25]2[F:26])[c:28]2[c:29]([F:35])[cH:30][cH:31][c:32]([F:34])[cH:33]2)[cH:14][cH:15]1.[cH:36]1[cH:37][cH:38][n:39][cH:40][cH:41]1>>[CH3:1][S:2](=[O:4])(=[O:5])[NH:27][c:22]1[cH:21][c:20]([CH:19]([S:16]([c:13]2[cH:12][cH:11][c:10]([Cl:9])[cH:15][cH:14]2)(=[O:17])=[O:18])[c:28]2[c:29]([F:35])[cH:30][cH:31][c:32]([F:34])[cH:33]2)[c:25]([F:26])[cH:24][n:23]1

Participants

6

Reactant 5

HCID 1049PyridineHCID 6344DichloromethaneHCID 8857Ethyl AcetateHCID 31297Methanesulfonyl chlorideHCID 23114619HCID 23114619, compound

Product 1

HCID 23114764HCID 23114764, compound

Sources & evidence

ORD record
ord-ac2f37f2859d4d258ff2b6c2d911a845
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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