Potassium Cation → HCID 57964930, compound

HRID 1565539Notes

Reaction equation

HRID 1565539 reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][CH:11]([n:14]2[n:15][cH:16][c:17]3[c:18]2[n:19][cH:20][n:21][c:22]3[Cl:23])[CH2:12][CH2:13]1.[C:32](=[O:33])([O-:34])[O-:35].[CH3:38][N:39]([CH3:40])[CH:41]=[O:42].[Cl:24][c:25]1[cH:26][c:27]([OH:31])[cH:28][n:29][cH:30]1.[K+:36].[K+:37]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][CH:11]([n:14]2[n:15][cH:16][c:17]3[c:18]2[n:19][cH:20][n:21][c:22]3[O:31][c:27]2[cH:26][c:25]([Cl:24])[cH:30][n:29][cH:28]2)[CH2:12][CH2:13]1

Participants

6

Reactant 5

HCID 813Potassium Cation2×HCID 6228DimethylformamideHCID 19660Carbonate IonHCID 5823053-Hydroxy-5-chloropyridineHCID 57964905Tert-butyl 4-(4-chloro-1H-pyrazolo[3,4-D]pyrimidin-1-YL)piperidine-1-carboxylate

Product 1

HCID 57964930HCID 57964930, compound

Sources & evidence

ORD record
ord-249da8f36c324f55a8884688ef2bf709
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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