Ammonium → HCID 57964899, compound

HRID 1147305Notes

Reaction equation

HRID 1147305 reaction equation
[C:10]([CH3:11])([CH3:12])([CH3:13])[O:14][C:15](=[O:16])[N:17]1[CH2:18][CH2:19][CH:20]([n:23]2[n:24][cH:25][c:26]3[c:27]2[n:28][cH:29][n:30][c:31]3[Cl:32])[CH2:21][CH2:22]1.[Cl-:33].[H-:1].[NH4+:34].[Na+:2].[O:35]=[CH:36][N:37]([CH3:38])[CH3:39].[OH:3][c:4]1[cH:5][cH:6][cH:7][cH:8][cH:9]1>>[O:3]([c:4]1[cH:5][cH:6][cH:7][cH:8][cH:9]1)[c:31]1[c:26]2[cH:25][n:24][n:23]([CH:20]3[CH2:19][CH2:18][N:17]([C:15]([O:14][C:10]([CH3:11])([CH3:12])[CH3:13])=[O:16])[CH2:22][CH2:21]3)[c:27]2[n:28][cH:29][n:30]1

Participants

8

Reactant 7

HCID 223AmmoniumHCID 312ChlorideHCID 923Sodium ionHCID 996PhenolHCID 6228DimethylformamideHCID 166653HydrideHCID 57964905Tert-butyl 4-(4-chloro-1H-pyrazolo[3,4-D]pyrimidin-1-YL)piperidine-1-carboxylate

Product 1

HCID 57964899HCID 57964899, compound

Sources & evidence

ORD record
ord-d738adf4f2eb4ed6bdba2165ef8bdcaa
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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