Potassium Cation → HCID 86662075, compound

HRID 98379Notes

Reaction equation

[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]([C:9]([O:10][C:11]([CH3:12])([CH3:13])[CH3:14])=[O:15])[c:16]1[n:17][cH:18][c:19]([N:28]2[CH2:29][CH2:30][N:31]([S:34](=[O:35])(=[O:36])[CH2:37][CH3:38])[CH2:32][CH2:33]2)[n:20][c:21]1[C:22]#[C:23][Si:24]([CH3:25])([CH3:26])[CH3:27].[CH3:45][OH:46].[K+:39].[K+:40].[O-:41][C:42]([O-:43])=[O:44]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]([C:9]([O:10][C:11]([CH3:12])([CH3:13])[CH3:14])=[O:15])[c:16]1[n:17][cH:18][c:19]([N:28]2[CH2:29][CH2:30][N:31]([S:34](=[O:35])(=[O:36])[CH2:37][CH3:38])[CH2:32][CH2:33]2)[n:20][c:21]1[C:22]#[CH:23]

Participants

Reactant 4

HCID 813Potassium Cation2×

HCID 887Methanol

HCID 19660Carbonate Ion

HCID 66745624Tert-butyl N-tert-butoxycarbonyl-5-(4-(ethylsulfonyl)piperazin-1-yl)-3-((trimethylsilyl)ethynyl)pyrazin-2-ylcarbamate

Product 1

HCID 86662075HCID 86662075, compound

Sources & evidence

ORD record: ord-0cfce3c0e84f46fdaa891bee89251755
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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