2-Chloroethyl isocyanate → 1-(2-Chloro-ethyl)-3-(2,6-dimethyl-pyridin-4-yl)-urea
Reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([NH2:8])[CH:5]=[C:4]([CH3:9])[N:3]=1.[Cl:10][CH2:11][CH2:12][N:13]=[C:14]=[O:15]>C1COCC1>[Cl:10][CH2:11][CH2:12][NH:13][C:14]([NH:8][C:6]1[CH:5]=[C:4]([CH3:9])[N:3]=[C:2]([CH3:1])[CH:7]=1)=[O:15]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2,6-Dimethyl-pyridin-4-ylamine (Example C1.2., 1.22 g, 10 mmol) is dissolved in dry THF (30 mL) and 1-chloro-2-isocyanato-ethane (1.06 g, 10 mmol) is added. The mixture is stirred at r.t. for 15 h. The mixture is evaporated and the residue purified by MPLC to provide the title compound.
Workup
- customThe mixture is evaporated
- customthe residue purified by MPLC
Sources & evidence
- ORD record
- ord-3dff6f7deb624cda9eab4aace40bcc7a
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07750161B2
Reaction notes
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