Hydrochloric Acid → HCID 21455284, compound
Reaction equation
[NH:1]([C:5]1[N:16]=[C:8]2[C:9]3[C:14]([CH2:15][N:7]2[N:6]=1)=[CH:13][CH:12]=[CH:11][CH:10]=3)[C:2]([NH2:4])=S.[OH:17]O.Cl>[OH-].[Na+]>[NH:1]([C:5]1[N:16]=[C:8]2[C:9]3[C:14]([CH2:15][N:7]2[N:6]=1)=[CH:13][CH:12]=[CH:11][CH:10]=3)[C:2]([NH2:4])=[O:17]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
2-Thioureido-5H-s-triazolo[5,1-a]isoindole (1.15 g, 0.005 mole) is suspended in 20 ml of 2% aqueous sodium hydroxide and 2.3 ml of 36% H2O2 (0.024 mole) is added at 40°-45° C. After 15 minutes, the mixture is heated for 5 minutes at 80° C then, after cooling and neutralizing with dilute hydrochloric acid, the resulting solid precipitate is recovered by filtration and is purified by crystallization from 60% ethanol. Yield 0.83 g; m.p. 261°-3° C.
Workup
- filtrationthe resulting solid precipitate is recovered by filtration
- customis purified by crystallization from 60% ethanol
Sources & evidence
- ORD record
- ord-70ca484c025543d6a0e0d3fc950a8185
- Source dataset
- uspto-grants-1977_02
- Patent number
- US04007276
Reaction notes
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