Hydrochloric Acid → HCID 178479551, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:4][C:3]=1[NH:12][C:13](=[O:32])[NH:14][C:15]1[CH:16]=[C:17]([CH:28]=[C:29]([F:31])[CH:30]=1)[CH2:18][NH:19][C:20]1[C:21]([C:25]([NH2:27])=[O:26])=[N:22][NH:23][CH:24]=1.Cl>C(O)C.C(OCC)C>[ClH:1].[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:10])([F:11])[F:9])[CH:5]=[CH:4][C:3]=1[NH:12][C:13](=[O:32])[NH:14][C:15]1[CH:16]=[C:17]([CH:28]=[C:29]([F:31])[CH:30]=1)[CH2:18][NH:19][C:20]1[C:21]([C:25]([NH2:27])=[O:26])=[N:22][NH:23][CH:24]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A suspension of 1.64 g (3.48 mmol) of 4-{3-[3-(2-chloro-4-trifluoromethylphenyl)ureido]-5-fluorobenzylamino}-1H-pyrazole-3-carboxamide in 50 ml of ethanol is stirred at ambient temperature under an argon atmosphere. Then 35 ml (35 mmol) of a solution of hydrochloric acid in diethyl ether (1 N) are added dropwise. The reaction medium becomes a clear solution. After stirring for 10 hours at ambient temperature, the solvents are evaporated using a rotary evaporator under reduced pressure. The residue obtained is stirred in 50 ml of diethyl ether for 30 minutes.
Workup
- stirringAfter stirring for 10 hours at ambient temperature
- customthe solvents are evaporated
- customa rotary evaporator under reduced pressure
- customThe residue obtained
Sources & evidence
- ORD record
- ord-86bc572ad5514e4192640ea56bec927e
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367715B2
Reaction notes
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