Pyridine → HCID 86611323, compound

HRID 688894Notes

Reaction equation

HRID 688894 reaction equation
[C:12](#[N:13])[c:14]1[c:15]([C:32]([F:33])([F:34])[F:35])[cH:16][c:17]([NH:20][C:21](=[O:22])[c:23]2[cH:24][cH:25][c:26]3[c:30]([cH:31]2)[NH:29][CH2:28][CH2:27]3)[cH:18][cH:19]1.[Cl:1][c:2]1[cH:3][c:4]([S:8](=[O:9])(=[O:10])[Cl:11])[cH:5][cH:6][cH:7]1.[Cl:42][CH2:43][Cl:44].[cH:36]1[cH:37][cH:38][n:39][cH:40][cH:41]1>>[Cl:1][c:2]1[cH:3][c:4]([S:8](=[O:9])(=[O:10])[N:29]2[CH2:28][CH2:27][c:26]3[cH:25][cH:24][c:23]([C:21]([NH:20][c:17]4[cH:16][c:15]([C:32]([F:33])([F:34])[F:35])[c:14]([C:12]#[N:13])[cH:19][cH:18]4)=[O:22])[cH:31][c:30]32)[cH:5][cH:6][cH:7]1

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 179093-Chlorobenzenesulphonyl chlorideHCID 86611322HCID 86611322, compound

Product 1

HCID 86611323HCID 86611323, compound

Sources & evidence

ORD record
ord-3c35942c24eb4be4b77334285368929e
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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