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Tetrahydrofuran → Tert-butyl 4-(2-oxo-1,2-dihydroquinazolin-3(4H)-YL)piperidine-1-carboxylate

HRID 110152
Notes
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Reaction equation

HRID 110152 reaction equation
[C:25](=[O:26])([n:27]1[cH:28][cH:29][n:30][cH:31]1)[n:32]1[cH:33][cH:34][n:35][cH:36]1.[CH2:43]1[O:44][CH2:45][CH2:46][CH2:47]1.[CH3:37][CH2:38][O:39][C:40]([CH3:41])=[O:42].[N+:1]([O-:2])(=[O:3])[c:4]1[c:5]([CH2:6][NH:7][CH:8]2[CH2:9][CH2:10][N:11]([C:14](=[O:15])[O:16][C:17]([CH3:18])([CH3:19])[CH3:20])[CH2:12][CH2:13]2)[cH:21][cH:22][cH:23][cH:24]1>>[NH:1]1[c:4]2[c:5]([cH:21][cH:22][cH:23][cH:24]2)[CH2:6][N:7]([CH:8]2[CH2:9][CH2:10][N:11]([C:14](=[O:15])[O:16][C:17]([CH3:18])([CH3:19])[CH3:20])[CH2:12][CH2:13]2)[C:25]1=[O:26]
ParticipantsSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 8028TetrahydrofuranHCID 8857Ethyl AcetateHCID 682631,1'-CarbonyldiimidazoleHCID 13046886tert-Butyl 4-{[(2-nitrophenyl)methyl]amino}piperidine-1-carboxylate

Product 1

HCID 53415303Tert-butyl 4-(2-oxo-1,2-dihydroquinazolin-3(4H)-YL)piperidine-1-carboxylate

Sources & evidence

ORD record
ord-f66b85341ffd490f8aa602e825bccbc8
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