Hydrochloric Acid → HCID 19939835, compound
Reaction equation
[Cl:1][C:2]1[N:11]=[C:10]2[C:5]([C:6](=[O:23])[C:7]([C:18]([O:20]CC)=[O:19])=[CH:8][N:9]2[C:12]2[C:16]([CH3:17])=[N:15][O:14][N:13]=2)=[CH:4][C:3]=1[F:24].Cl.O>C(O)(=O)C>[Cl:1][C:2]1[N:11]=[C:10]2[C:5]([C:6](=[O:23])[C:7]([C:18]([OH:20])=[O:19])=[CH:8][N:9]2[C:12]2[C:16]([CH3:17])=[N:15][O:14][N:13]=2)=[CH:4][C:3]=1[F:24]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
Compound No. 78 (30 mg) obtained in Example 39 was dissolved in acetic acid (2 ml ) and 6N-HCl (0.5 ml). The solution was stirred at 100° C. for 0.5 hour. After cooling and addition of water (10 ml), the precipitate was filtrated and washed with ethanol and ether. The title compound No. 79 was obtained as a colorless solid (5 mg).
Workup
- temperatureAfter cooling
- filtrationthe precipitate was filtrated
- washwashed with ethanol and ether
Sources & evidence
- ORD record
- ord-69acfc675a8a426da270e4e08b402afe
- Source dataset
- uspto-grants-1995_05
- Patent number
- US05412098
Reaction notes
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