Methyl isothiocyanate → HCID 9970424, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=2)=[CH:4][CH:3]=1.[CH3:16][N:17]=[C:18]=[S:19]>C(O)C>[CH3:16][NH:17][C:18](=[S:19])[NH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=2)=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2-[2-(4-aminophenyl)ethyl]pyridine (5.8 g) and methyl isothiocyanate (2.6 g) in ethanol (60 ml) was refluxed for one hour. The reaction mixture was evaporated in vacuo to give a crystalline residue, which was recrystallized from a mixture of ethyl acetate and diisopropyl ether to give 2-[2-{4-(3-methylthioureido)phenyl}ethyl]pyridine (7.3 g).
Workup
- customThe reaction mixture was evaporated in vacuo
- customto give a crystalline residue, which
- customwas recrystallized from a mixture of ethyl acetate and diisopropyl ether
Sources & evidence
- ORD record
- ord-2786915190ab40a69fda641934215733
- Source dataset
- uspto-grants-1991_09
- Patent number
- US05047411
Reaction notes
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