Hydrazine hydrate (1:1) → HCID 178427940, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([NH:8][C:9](=[NH:12])SC)[CH:5]=[C:4]([Cl:13])[C:3]=1[CH3:14].[NH2:15][NH2:16].O>C(O)C>[Cl:1][C:2]1[CH:7]=[C:6]([NH:8][C:9]([NH2:12])=[N:15][NH2:16])[CH:5]=[C:4]([Cl:13])[C:3]=1[CH3:14]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To 7.18 g of 1-(2,6-dichloro-4-tolyl)-2-methylisothiourea.HJ (C), suspended in 26 ml of ethanol, 1.3 ml of hydrazine.hydrate is added after which the mixture is refluxed for 20 hours. The precipitate formed is filtered off and the filtrate evaporated to dryness. Yield: 6.35 g. Melting point HJ salt: 203°-205° C; melting point HCl salt: 149°-150° C.
Workup
- temperatureis refluxed for 20 hours
- customThe precipitate formed
- filtrationis filtered off
- customthe filtrate evaporated to dryness
- custom203°-205° C
- custom149°-150° C.
Sources & evidence
- ORD record
- ord-2f6520e31cb04f728e46a2695e9c7050
- Source dataset
- uspto-grants-1978_07
- Patent number
- US04101675
Reaction notes
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