Methyl isothiocyanate → HCID 178486120, compound

HRID 2397683Notes

Reaction equation

HRID 2397683 reaction equation
C(=O)([O-])[O-].[K+].[K+].Cl.Cl.[CH3:9][C:10]1[N:11]=[CH:12][NH:13][C:14]=1[CH2:15][S:16][CH2:17][CH2:18][NH2:19].[CH3:20][N:21]=[C:22]=[S:23]>O>[CH3:20][NH:21][C:22]([NH:19][CH2:18][CH2:17][S:16][CH2:15][C:14]1[NH:13][CH:12]=[N:11][C:10]=1[CH3:9])=[S:23]

Participants

5

Reactant 3

HCID 11167Methyl isothiocyanateHCID 11430Potassium CarbonateHCID 30159992-(((5-Methyl-1H-imidazol-4-yl)methyl)thio)ethylamine dihydrochloride

Product 1

HCID 178486120HCID 178486120, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

(i) Potassium carbonate (7.75 g.) was added to a solution of 4-methyl-5-[(2-aminoethyl)thiomethyl]imidazole dihydrochloride (14.6 g.) in water (120 ml.). The solution was stirred at room temperature for 15 minutes and methyl isothiocyanate (5.15 g.) was added. After heating under reflux for 30 minutes, the solution was slowly cooled to 5°. The product (13.1 g.) was collected and recrystallised from water to give N-methyl-N'-[2-((4-methyl-5-imidazolyl)methylthio)ethyl]thiourea, m.p. 150°-152°.

Workup

  1. temperatureAfter heating
  2. temperatureunder reflux for 30 minutes
  3. temperaturethe solution was slowly cooled to 5°
  4. customThe product (13.1 g.) was collected
  5. customrecrystallised from water

Sources & evidence

ORD record
ord-1accb6b98fdc435c803836548c5051a7
Source dataset
uspto-grants-1977_05
Patent number
US04022797

Reaction notes

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