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Potassium Cation → Tert-butyl 4-(4-bromo-3-cyanopyrazol-1-yl)piperidine-1-carboxylate

HRID 1547305
Notes
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Reaction equation

HRID 1547305 reaction equation
[Br:1][c:2]1[c:3]([C:7]#[N:8])[nH:4][n:5][cH:6]1.[C:9](=[O:10])([O-:11])[O-:12].[CH3:15][S:16]([O:17][CH:20]1[CH2:21][CH2:22][N:23]([C:26](=[O:27])[O:28][C:29]([CH3:30])([CH3:31])[CH3:32])[CH2:24][CH2:25]1)(=[O:18])=[O:19].[CH3:33][C:34]#[N:35].[K+:13].[K+:14]>>[Br:1][c:2]1[c:3]([C:7]#[N:8])[n:4][n:5]([CH:20]2[CH2:21][CH2:22][N:23]([C:26](=[O:27])[O:28][C:29]([CH3:30])([CH3:31])[CH3:32])[CH2:24][CH2:25]2)[cH:6]1
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 813Potassium Cation2×HCID 6342AcetonitrileHCID 19660Carbonate IonHCID 27356234-Bromo-1H-pyrazole-3-carbonitrileHCID 41848691-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine

Product 1

HCID 67388412Tert-butyl 4-(4-bromo-3-cyanopyrazol-1-yl)piperidine-1-carboxylate

Sources & evidence

ORD record
ord-8447d9c9465c4e8fbf03888e12d9955b
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes