3-(4-Nitrobenzyl)imidazolidine-2,4-dione → HCID 10655843, compound

HRID 1059826Notes

Reaction equation

HRID 1059826 reaction equation
[N+:1]([C:4]1[CH:17]=[CH:16][C:7]([CH2:8][N:9]2[C:13](=[O:14])[CH2:12][NH:11][C:10]2=[O:15])=[CH:6][CH:5]=1)([O-])=O>CO.[Pd].[H][H]>[NH2:1][C:4]1[CH:17]=[CH:16][C:7]([CH2:8][N:9]2[C:13](=[O:14])[CH2:12][NH:11][C:10]2=[O:15])=[CH:6][CH:5]=1

Participants

5

Reactant 1

HCID 107522073-(4-Nitrobenzyl)imidazolidine-2,4-dione

Product 1

HCID 10655843HCID 10655843, compound

Reagents, catalysts & solvents 3

HCID 887MethanolSolventHCID 23938PalladiumSolventHCID 178418361HCID 178418361, compoundSolvent

Procedure

The 3-(4-nitrobenzyl)hydantoin derivative was dissolved in methanol (about 10 ml per mmol of hydantoin derivative) and hydrogenated with palladium/carbon in a hydrogen atmosphere until reaction was complete. The catalyst was filtered off and the solvent was removed on a rotary evaporator. The 3-(4-aminobenzyl)hydantoin derivative was obtained.

Workup

  1. filtrationThe catalyst was filtered off
  2. customthe solvent was removed on a rotary evaporator

Sources & evidence

ORD record
ord-9543fc1f62c74d88a04e4c1b76e10261
Source dataset
uspto-grants-2003_02
Patent number
US06521654B2

Reaction notes

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