Potassium Cation → HCID 57964998, compound

HRID 2312933Notes

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:34](=[O:35])([O-:36])[O-:37].[K+:38].[K+:39].[OH:24][c:25]1[cH:26][c:27]2[cH:28][cH:29][nH:30][c:31]2[cH:32][cH:33]1>>[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:24][c:25]2[cH:26][c:27]3[cH:28][cH:29][nH:30][c:31]3[cH:32][cH:33]2)[CH2:12][CH2:13]1

Participants

Reactant 4

HCID 813Potassium Cation2×

HCID 160545-Hydroxyindole

HCID 19660Carbonate Ion

HCID 57964905Tert-butyl 4-(4-chloro-1H-pyrazolo[3,4-D]pyrimidin-1-YL)piperidine-1-carboxylate

Product 1

HCID 57964998HCID 57964998, compound

Sources & evidence

ORD record: ord-e2cd67ff7a9a411493a03be29852c2f9
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI: 10.1039/C8SC04228D

Reaction notes

Loading…