Potassium Cation → HCID 57099041, compound

HRID 203376Notes

Reaction equation

HRID 203376 reaction equation
[C:16]([CH3:17])([CH3:18])([CH3:19])[n:20]1[n:21][cH:22][c:23]([SH:28])[c:24]([Cl:27])[c:25]1=[O:26].[C:29](=[O:30])([O-:31])[O-:32].[CH3:35][N:36]([CH3:37])[CH:38]=[O:39].[Cl:1][C:2](=[CH:3][c:4]1[cH:5][cH:6][c:7]([CH2:8][Br:9])[cH:10][cH:11]1)[C:12]([F:13])([F:14])[F:15].[K+:33].[K+:34]>>[Cl:1][C:2](=[CH:3][c:4]1[cH:5][cH:6][c:7]([CH2:8][S:28][c:23]2[cH:22][n:21][n:20]([C:16]([CH3:17])([CH3:18])[CH3:19])[c:25](=[O:26])[c:24]2[Cl:27])[cH:10][cH:11]1)[C:12]([F:13])([F:14])[F:15]

Participants

6

Reactant 5

HCID 813Potassium Cation2×HCID 6228DimethylformamideHCID 19660Carbonate IonHCID 134692424-Chloro-2-(1,1-dimethylethyl)-5-mercapto-3(2H)-pyridazinoneHCID 537438994-(2-Chloro-3,3,3-trifluoroprop-1-enyl)-benzyl bromide

Product 1

HCID 57099041HCID 57099041, compound

Sources & evidence

ORD record
ord-a0ca98de95514805a26219acc65191ab
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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