Pyridine → HCID 21224903, compound

HRID 150746Notes

Reaction equation

HRID 150746 reaction equation
[Cl:43][CH2:44][Cl:45].[N+:31](=[O:32])([O-:33])[c:34]1[cH:35][cH:36][c:37]([C:38](=[O:39])[Cl:40])[cH:41][cH:42]1.[c:1]1(-[c:7]2[nH:8][c:9](=[O:24])[n:10]([S:12](=[O:13])(=[O:14])[c:15]3[cH:16][c:17]4[c:21]([cH:22][cH:23]3)[NH:20][CH2:19][CH2:18]4)[cH:11]2)[cH:2][cH:3][cH:4][cH:5][cH:6]1.[cH:25]1[cH:26][cH:27][n:28][cH:29][cH:30]1>>[c:1]1(-[c:7]2[nH:8][c:9](=[O:24])[n:10]([S:12](=[O:13])(=[O:14])[c:15]3[cH:16][c:17]4[c:21]([cH:22][cH:23]3)[N:20]([C:38]([c:37]3[cH:36][cH:35][c:34]([N+:31](=[O:32])[O-:33])[cH:42][cH:41]3)=[O:39])[CH2:19][CH2:18]4)[cH:11]2)[cH:2][cH:3][cH:4][cH:5][cH:6]1

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 85024-Nitrobenzoyl chlorideHCID 11002343HCID 11002343, compound

Product 1

HCID 21224903HCID 21224903, compound

Sources & evidence

ORD record
ord-af10387818c245a1b1d4eb07c047b483
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

Loading…