CH2N2Pb → HCID 178433311, compound

HRID 2166716Notes

Reaction equation

HRID 2166716 reaction equation
[N:1]#[C:2][NH2:3].[Pb].[CH3:5][C:6]1[N:7]=[CH:8][NH:9][C:10]=1[CH2:11][S:12][CH2:13][CH2:14][NH:15][C:16]([NH:18][CH2:19][CH2:20][S:21][CH2:22][C:23]1[NH:27][CH:26]=[N:25][C:24]=1[CH3:28])=S>C(#N)C.CN(C)C=O>[C:2]([NH:3][C:16]([NH:15][CH2:14][CH2:13][S:12][CH2:11][C:10]1[NH:9][CH:8]=[N:7][C:6]=1[CH3:5])=[N:18][CH2:19][CH2:20][S:21][CH2:22][C:23]1[NH:27][CH:26]=[N:25][C:24]=1[CH3:28])#[N:1]

Participants

5

Reactant 2

HCID 22262466CH2N2Pb2×HCID 178433325HCID 178433325, compound

Product 1

HCID 178433311HCID 178433311, compound

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideSolventHCID 6342AcetonitrileSolvent

Procedure

Lead cyanamide (8.7 g.) was added to a solution of N,N'-bis-[2-((4-methyl-5-imidazolyl)methylthio)ethyl]thiourea in acetonitrile (100 ml.) and dimethyl formamide (20 ml.) and the resultant suspension was heated under reflux with stirring for 24 hours. Additional lead cyanamide (8.7 g.) was added and heating was continued for 24 hours. Following filtration and concentration, the residue was chromatographed on a column of silica gel, eluting with ethyl acetate-isopropyl alcohol (5:1). Recrystallisation from isopropyl alcohol-isopropyl acetate afforded N-cyano-N',N"-bis-[2-((4-methyl-5-imidazolyl)methylthio)ethyl]guanidine (0.6 g.), m.p. 92°-95°.

Workup

  1. temperatureunder reflux
  2. temperatureheating
  3. waitwas continued for 24 hours
  4. filtrationfiltration and concentration
  5. customthe residue was chromatographed on a column of silica gel
  6. washeluting with ethyl acetate-isopropyl alcohol (5:1)
  7. customRecrystallisation from isopropyl alcohol-isopropyl acetate

Sources & evidence

ORD record
ord-c07aef83a0d5497e9e35dab6f304d22e
Source dataset
uspto-grants-1983_06
Patent number
US04388319

Reaction notes

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