Methyl isothiocyanate → HCID 178486106, compound
Reaction equation
[NH2:1][C:2]1[CH2:6][CH2:5][N:4]([C:7]2[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][CH:8]=2)[N:3]=1.[CH3:14][N:15]=[C:16]=[S:17]>>[CH3:14][NH:15][C:16](=[S:17])[NH:1][C:2]1[CH2:6][CH2:5][N:4]([C:7]2[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][CH:8]=2)[N:3]=1Participants
3
Procedure
3-Amino-1-(4-chlorophenyl)-2-pyrazoline (1.5 g) (prepared in Reference Example 6 of our European patent specification No. 22-578) and methylisothiocyanate (1.02 g) were heated together at 100° for two hours. The crude product was ground under methanol, collected by filtration, and recrystallised from acetone to yield 3-(3-methylthioureido)-1-(4-chlorophenyl)-2-pyrazoline, m.p. 237°.
Workup
- filtrationcollected by filtration
- customrecrystallised from acetone
Sources & evidence
- ORD record
- ord-f7322818cc2c48fba8a956de47e50faf
- Source dataset
- uspto-grants-1984_08
- Patent number
- US04465685
Reaction notes
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