Methyl Isocyanate → HCID 13498706, compound
Reaction equation
[NH2:1][CH2:2][CH2:3][S:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][N:7]=1.[CH3:12][N:13]=[C:14]=[O:15]>C(#N)C>[CH3:12][NH:13][C:14]([NH:1][CH2:2][CH2:3][S:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][N:7]=1)=[O:15]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 2-[(2-aminoethyl)thiomethyl]pyridine (7.0 g.) and methyl isocyanate (2.7 g.) in acetonitrile was heated for 18 hours in a pressure vessel at 100°. After cooling, the solid obtained was collected and recrystallised from acetonitrile/ether to give N-methyl-N'-[2-(2-pyridylmethylthio)ethyl]urea m.p. 63°-66°.
Workup
- temperaturewas heated for 18 hours in a pressure vessel at 100°
- temperatureAfter cooling
- customthe solid obtained
- customwas collected
- customrecrystallised from acetonitrile/ether
Sources & evidence
- ORD record
- ord-b26e5ea485314a2c933f0e9b11792995
- Source dataset
- uspto-grants-1977_05
- Patent number
- US04027026
Reaction notes
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