Hydrazine → HCID 20333332, compound
Reaction equation
CS([C:5]1[N:10]=[C:9]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([C:17]([F:20])([F:19])[F:18])[CH:12]=2)[CH:8]=[CH:7][N:6]=1)(=O)=O.[NH2:21][NH2:22]>C(O)C>[NH:21]([C:5]1[N:10]=[C:9]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([C:17]([F:20])([F:19])[F:18])[CH:12]=2)[CH:8]=[CH:7][N:6]=1)[NH2:22]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 6.0 g. of 2-methylsulfonyl-4-(m-trifluoromethylphenyl)pyrimidine in 75 ml. of absolute ethanol is treated with 1.9 g. of 95% hydrazine and is refluxed for 8 hours. Isolation as in the previous example gives the desired compound, m.p. 103°-106° C.; resolidifies and melts at 120°-122° C.
Sources & evidence
- ORD record
- ord-cc22e2cf01104d9db4c6406aca69b651
- Source dataset
- uspto-grants-1980_06
- Patent number
- US04209621
Reaction notes
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