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Phosphorus sulfide (P2S5) → HCID 20064187, compound

HRID 359705
Notes
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Reaction equation

HRID 359705 reaction equation
[O:1]=[C:2]1[NH:6][C:5]([CH3:7])=[C:4]([C:8]([N:10]([CH3:12])[CH3:11])=O)[NH:3]1.P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:14]>N1C=CC=CC=1.O>[O:1]=[C:2]1[NH:6][C:5]([CH3:7])=[C:4]([C:8](=[S:14])[N:10]([CH3:12])[CH3:11])[NH:3]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 14817Phosphorus sulfide (P2S5)HCID 128502882,3-Dihydro-2-oxo-4,N,N-trimethyl-1H-imidazole-5-carboxamide

Product 1

HCID 20064187HCID 20064187, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 1049PyridineSolvent

Procedure

A suspension of 3.4 g (20 mmol) of 2,3-dihydro--N,N,5-trimethyl-2-oxo-1H-imidazole-4-carboxamide (prepared in example 3) and 4.4 g cf phosphorus pentasulfide in 100 ml of dry pyridine is stirred at reflux temperature for 6 hours. The mixture is allowed to cool overnight and is diluted with water. The precipitate is collected and recrystallized from 50% aqueous ethanol to give the title compound.

Workup

  1. temperatureat reflux temperature for 6 hours
  2. temperatureto cool overnight
  3. customThe precipitate is collected
  4. customrecrystallized from 50% aqueous ethanol

Sources & evidence

ORD record
ord-d4b06bb8ef694eeca746dd9a717b2ddf
Source dataset
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05002961

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes