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Potassium Cation → tert-Butyl 4-[(6-bromo-1-oxo-1,2-dihydroisoquinolin-4-yl)sulfanyl]piperidine-1-carboxylate

HRID 314872
Notes
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Reaction equation

HRID 314872 reaction equation
[Br:1][c:2]1[cH:3][c:4]2[c:5]([SH:13])[cH:6][nH:7][c:8](=[O:12])[c:9]2[cH:10][cH:11]1.[C:32](=[O:33])([O-:34])[O-:35].[CH3:14][S:15]([O:16][CH:19]1[CH2:20][CH2:21][N:22]([C:25](=[O:26])[O:27][C:28]([CH3:29])([CH3:30])[CH3:31])[CH2:23][CH2:24]1)(=[O:17])=[O:18].[K+:36].[K+:37]>>[Br:1][c:2]1[cH:3][c:4]2[c:5]([S:13][CH:19]3[CH2:20][CH2:21][N:22]([C:25](=[O:26])[O:27][C:28]([CH3:29])([CH3:30])[CH3:31])[CH2:23][CH2:24]3)[cH:6][nH:7][c:8](=[O:12])[c:9]2[cH:10][cH:11]1
ParticipantsSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 813Potassium Cation2×HCID 19660Carbonate IonHCID 41848691-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 57439914HCID 57439914, compound

Product 1

HCID 67130258tert-Butyl 4-[(6-bromo-1-oxo-1,2-dihydroisoquinolin-4-yl)sulfanyl]piperidine-1-carboxylate

Sources & evidence

On this pageParticipantsSources & evidenceReaction notes
ORD record
ord-110fed16c31c4eab9a54cd9394091c30
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI
10.1039/C8SC04228D

Reaction notes

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