Hydrochloric Acid → HCID 131724853, compound
Reaction equation
[ClH:1].[S:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[C:7]([O:9][CH:10]1[CH:24]([N:25]([CH3:27])[CH3:26])[C:23]2=[CH:28][CH:20]([O:21][C:22]2=[O:29])[CH:19]2[CH:15]([O:16][C:17](=[O:31])[CH:18]2[CH3:30])[CH2:14][C:13]2([CH3:32])[CH:11]1[O:12]2)=[O:8]>CC(C)=O>[ClH:1].[S:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[C:7]([O:9][CH:10]1[CH:24]([N:25]([CH3:27])[CH3:26])[C:23]2=[CH:28][CH:20]([O:21][C:22]2=[O:29])[CH:19]2[CH:15]([O:16][C:17](=[O:31])[CH:18]2[CH3:30])[CH2:14][C:13]2([CH3:32])[CH:11]1[O:12]2)=[O:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of hydrochloric acid (0.8 mmol; 0.8 ml; 1N in ether) is added to a solution of the compound of Example 29 (0.44 mmol; 196 mg) in acetone (4 ml). The precipitate is filtered, washed with a little acetone, with ether and dried under reduced pressure. 180 mg of the expected product is obtained in the form of a white powder.
Workup
- filtrationThe precipitate is filtered
- washwashed with a little acetone, with ether
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-3ac911f59f954970ad3ec37e4b448092
- Source dataset
- uspto-grants-2005_05
- Patent number
- US06887869B2
Reaction notes
Loading…