Hydrochloric Acid → HCID 178514068, compound
Reaction equation
[F:1][C:2]([F:36])([F:35])[C:3]1[CH:4]=[C:5]([N:9]([C:13]2[CH:18]=[CH:17][C:16]([C:19]3[CH:24]=[CH:23][C:22]([C:25]([O:27]CC)=[O:26])=[CH:21][CH:20]=3)=[CH:15][C:14]=2[C:30]2[NH:34][N:33]=[N:32][N:31]=2)[C:10]([NH2:12])=[O:11])[CH:6]=[CH:7][CH:8]=1.[OH-].[Na+].Cl>C(O)C>[F:36][C:2]([F:1])([F:35])[C:3]1[CH:4]=[C:5]([N:9]([C:13]2[CH:18]=[CH:17][C:16]([C:19]3[CH:20]=[CH:21][C:22]([C:25]([OH:27])=[O:26])=[CH:23][CH:24]=3)=[CH:15][C:14]=2[C:30]2[NH:34][N:33]=[N:32][N:31]=2)[C:10]([NH2:12])=[O:11])[CH:6]=[CH:7][CH:8]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 3-trifluoromethylphenyl-4-(4-ethoxycarbonylphenyl)-2-(5-tetrazolyl)phenyl urea (4.5 g, 9 mmol) in 96% ethanol was added sodium hydroxide (4 N, 25 mL). The reaction was heated to reflux for 30 min, then cooled to room temperature and acidified with hydrochloric acid. The precipitate was filtered off to give 3.8 g of the desired material. M.p. 300° C. (dec.).
Workup
- temperatureThe reaction was heated
- temperatureto reflux for 30 min
- filtrationThe precipitate was filtered off
Sources & evidence
- ORD record
- ord-4f15f70a19c6432eb2b141d2b5e3b43d
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06696475B2
Reaction notes
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