Hydrochloric Acid → HCID 70212384, compound
Reaction equation
[F:1][C:2]([F:29])([F:28])[S:3]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][N:14]2[C:24](=[O:25])[C:23]3[N:26]4[C:16](=[CH:17][N:18]=[C:19]4[CH:20]=[CH:21][CH:22]=3)[C:15]2=[O:27])=[CH:9][CH:8]=1)(=[O:5])=[O:4].[ClH:30]>CO>[ClH:30].[F:28][C:2]([F:1])([F:29])[S:3]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][N:14]2[C:24](=[O:25])[C:23]3[N:26]4[C:16](=[CH:17][N:18]=[C:19]4[CH:20]=[CH:21][CH:22]=3)[C:15]2=[O:27])=[CH:9][CH:8]=1)(=[O:4])=[O:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 129 mg (0.30 mmol) of 4,5-dihydro-4-[4-(trifluoromethanesulfonamido) phenylmethyl]-3H-1,4,8b-triazaacenaphthylene-3,5-dione in 10 ml of methanol was added 0.04 ml of conc. HCl. The solvent was distilled off. To the residue was added acetone. The resulting solid was washed with acetone and dried to afford 141 mg of the desired compound (100%, a pale brown solid).
Workup
- distillationThe solvent was distilled off
- additionTo the residue was added acetone
- washThe resulting solid was washed with acetone
- customdried
Sources & evidence
- ORD record
- ord-cc82c3653f934a59a6c323cc70f49f73
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06251905B1
Reaction notes
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