Dimethylformamide → N-cyano-N'-[2-(3-isothiazolylmethylthio)ethyl]-N"-methylguanidine

HRID 1974415Notes

Reaction equation

HRID 1974415 reaction equation
[N:1]#[C:2][NH2:3].[Pb].[CH3:5][NH:6][C:7]([NH:9][CH2:10][CH2:11][S:12][CH2:13][C:14]1[CH:18]=[CH:17][S:16][N:15]=1)=S.CN(C)C=O>C(#N)C>[C:2]([NH:3][C:7]([NH:9][CH2:10][CH2:11][S:12][CH2:13][C:14]1[CH:18]=[CH:17][S:16][N:15]=1)=[N:6][CH3:5])#[N:1]

Participants

5

Reactant 3

HCID 6228DimethylformamideHCID 20466672N-Methyl-N'-(2-{[(1,2-thiazol-3-yl)methyl]sulfanyl}ethyl)thioureaHCID 22262466CH2N2Pb

Product 1

HCID 9992541N-cyano-N'-[2-(3-isothiazolylmethylthio)ethyl]-N"-methylguanidine

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

Lead cyanamide (52.6 g) was added to a solution of N-methyl-N'-[2-(3-isothiazolylmethylthio)ethyl]thiourea (17.7 g) in acetonitrile (500 ml) containing dimethylformamide (50 ml). The mixture was stirred under reflux for 48 hours, then filtered and concentrated. The product was chromatographed on silica gel with ethyl acetate as eluant and recrystallised from isopropyl acetate-ether to give N-cyano-N'-[2-(3-isothiazolylmethylthio)ethyl]-N"-methylguanidine, in a crystalline form, m.p.. 63°-64°. Further recrystallisation from isopropyl acetate afforded the cyanoguanidine in a crystalline form, m.p. 91°-92°.

Workup

  1. temperatureunder reflux for 48 hours
  2. filtrationfiltered
  3. concentrationconcentrated
  4. customThe product was chromatographed on silica gel with ethyl acetate as eluant
  5. customrecrystallised from isopropyl acetate-ether

Sources & evidence

ORD record
ord-f10fa382955b4a959672ebcccb4ed7ec
Source dataset
uspto-grants-1976_12
Patent number
US04000302

Reaction notes

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