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Potassium Cation → Tert-butyl 5-(2-oxo-1-piperidinyl)-1-indolinecarboxylate

HRID 109135
Notes
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Reaction equation

HRID 109135 reaction equation
[Br:18][CH2:19][CH2:20][CH2:21][CH2:22][C:23](=[O:24])[Cl:25].[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][c:11]2[cH:12][c:13]([NH2:17])[cH:14][cH:15][c:16]21.[CH2:32]1[O:33][CH2:34][CH2:35][CH2:36]1.[CH3:26][C:27]([CH3:28])([O-:29])[CH3:30].[K+:31]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][c:11]2[cH:12][c:13]([N:17]3[CH2:19][CH2:20][CH2:21][CH2:22][C:23]3=[O:24])[cH:14][cH:15][c:16]21
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 813Potassium CationHCID 8028TetrahydrofuranHCID 5211735-Bromovaleryl chlorideHCID 45749132-Methylpropan-2-olateHCID 22240520tert-Butyl 5-amino-2,3-dihydro-1H-indole-1-carboxylate

Product 1

HCID 22240498Tert-butyl 5-(2-oxo-1-piperidinyl)-1-indolinecarboxylate

Sources & evidence

ORD record
ord-b43b539268f84afb88f3d0307da27a23
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes