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Phenytoin → 5-Isopropylhydantoin

HRID 865708
Notes
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Reaction equation

HRID 865708 reaction equation
N1C2C(=CC=CC=2)C=C1CC1NC(=O)NC1=O.[C:18]1([C:24]2(C3C=CC=CC=3)[NH:28][C:27](=[O:29])[NH:26][C:25]2=[O:30])[CH:23]=CC=C[CH:19]=1.C(N1C(=O)C(C)NC1=O)CCC.C(N1C(=O)C(CC2C=CC=CC=2)NC1=O)CCC.C(N1C(=O)CNC1=O)CCC>>[CH3:19][CH:18]([CH:24]1[NH:28][C:27](=[O:29])[NH:26][C:25]1=[O:30])[CH3:23]
ParticipantsProcedureSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 1775PhenytoinHCID 3354773-Butyl-5-methylimidazolidine-2,4-dioneHCID 3591483-Butyl-5-(phenylmethyl)-2,4-imidazolidinedioneHCID 5682353-Butylimidazolidine-2,4-dioneHCID 219723355-(1H-indol-2-ylmethyl)-2,4-imidazolidinedione

Product 1

HCID 1030335-Isopropylhydantoin

Procedure

5-(1H-indol-2-ylmethyl)-2,4-imidazolidinedione; 5,5-diphenyl-2,4-imidazolidinedione; 3-butyl-5-methyl-2,4-imidazolidinedione; 3-butyl-5-(phenylmethyl)-2,4-imidazolidinedione; 3-butyl-2,4-imidazolidinedione,

Sources & evidence

ORD record
ord-d2184b7e8bf346c1b1d61ca4b9cd1536
Source dataset
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05567391

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes