Pyridine → HCID 22725169, compound

HRID 118583Notes

Reaction equation

HRID 118583 reaction equation
[Cl:1][C:2](=[O:3])[O:4][c:5]1[cH:6][cH:7][c:8]([N+:11](=[O:12])[O-:13])[cH:9][cH:10]1.[Cl:41][CH2:42][Cl:43].[F:14][c:15]1[cH:16][c:17]([CH:23]2[C:24]([C:32]([CH3:33])=[O:34])=[C:25]([CH3:31])[N:26]=[C:27]([O:29][CH3:30])[NH:28]2)[cH:18][c:19]([F:22])[c:20]1[F:21].[cH:35]1[cH:36][cH:37][n:38][cH:39][cH:40]1>>[C:2](=[O:3])([O:4][c:5]1[cH:6][cH:7][c:8]([N+:11](=[O:12])[O-:13])[cH:9][cH:10]1)[N:28]1[CH:23]([c:17]2[cH:16][c:15]([F:14])[c:20]([F:21])[c:19]([F:22])[cH:18]2)[C:24]([C:32]([CH3:33])=[O:34])=[C:25]([CH3:31])[N:26]=[C:27]1[O:29][CH3:30]

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 821294-Nitrophenyl chloroformateHCID 178494173HCID 178494173, compound

Product 1

HCID 22725169HCID 22725169, compound

Sources & evidence

ORD record
ord-577fffc7329f4733b9623cacbde56cbc
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction notes

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