2-Methyl-2H-pyrazol-3-ylamine → 5-Isothiocyanato-1-methyl-1H-pyrazole
Reaction equation
NC1N(C)N=CC=1.[CH3:8][N:9]1[C:13]([NH:14][C:15](=S)[SH:16])=[CH:12][CH:11]=[N:10]1>C(N(CC)CC)C>[CH3:8][N:9]1[C:13]([N:14]=[C:15]=[S:16])=[CH:12][CH:11]=[N:10]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Using 5-amino-1-methylpyrazole as a starting material, triethylamine salt of 1-methyl-5-pyrazolyldithiocarbamic acid (m.p.: 89° to 94° C.) was synthesized, following the procedures described in Reference Example 1. Ferric chloride was allowed to act upon the resulting product to yield the desired compound. Oily substance.
Workup
- customwas synthesized
Sources & evidence
- ORD record
- ord-e74b165e0c4145af816638c1f38bf441
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04830660
Reaction notes
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