Pyridine → HCID 69630494, compound

HRID 1543830Notes

Reaction equation

HRID 1543830 reaction equation
[Cl:24][c:25]1[c:26]([S:31](=[O:32])(=[O:33])[Cl:34])[cH:27][cH:28][cH:29][cH:30]1.[Cl:41][CH2:42][Cl:43].[NH2:1][c:2]1[cH:3][c:4]([N:11]2[CH2:12][CH2:13][N:14]([C:17](=[O:18])[O:19][C:20]([CH3:21])([CH3:22])[CH3:23])[CH2:15][CH2:16]2)[c:5]2[c:6]([cH:7][cH:8][o:9]2)[cH:10]1.[cH:35]1[cH:36][cH:37][n:38][cH:39][cH:40]1>>[NH:1]([c:2]1[cH:3][c:4]([N:11]2[CH2:12][CH2:13][N:14]([C:17](=[O:18])[O:19][C:20]([CH3:21])([CH3:22])[CH3:23])[CH2:15][CH2:16]2)[c:5]2[c:6]([cH:7][cH:8][o:9]2)[cH:10]1)[S:31]([c:26]1[c:25]([Cl:24])[cH:30][cH:29][cH:28][cH:27]1)(=[O:32])=[O:33]

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 761872-Chlorobenzenesulfonyl chlorideHCID 21864857HCID 21864857, compound

Product 1

HCID 69630494HCID 69630494, compound

Sources & evidence

ORD record
ord-244fe19bc0d240d88b4349a3a3cb30c3
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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