Methyl iodide → HCID 18952165, compound
Reaction equation
[CH3:1][NH:2][C:3]([NH:5][C:6]1[CH:11]=[C:10]([CH3:12])[CH:9]=[CH:8][C:7]=1[N:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1)=[S:4].[CH3:19][I:20]>CC(C)=O>[IH:20].[CH3:19][S:4][C:3](=[N:2][CH3:1])[NH:5][C:6]1[CH:11]=[C:10]([CH3:12])[CH:9]=[CH:8][C:7]=1[N:13]1[CH2:14][CH2:15][O:16][CH2:17][CH2:18]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 1-methyl-3-(5-methyl-2-morpholinophenyl)thiourea (6.4 g) and methyl iodide (3.8 g) in acetone (60 ml) was heated at reflux for 4 hours to give 2-methyl-1-(5-methyl-2-morpholinophenyl)-3-methyl-2-thiopseudourea hydroiodide as a pale yellow solid (m.p. 160°-161° C.).
Workup
- temperaturewas heated
- temperatureat reflux for 4 hours
Sources & evidence
- ORD record
- ord-7ef48c19716d4b75bfc96073dffe60fb
- Source dataset
- uspto-grants-1994_12
- Patent number
- US05373008
Reaction notes
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