Hydrochloric Acid → HCID 67369924, compound
Reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][N:11]2[CH2:16][CH2:15][C:14]([CH2:18][N:19]([CH3:30])[C:20]3[CH:28]=[CH:27][C:23]([C:24]([OH:26])=[O:25])=[CH:22][C:21]=3[CH3:29])([OH:17])[CH2:13][CH2:12]2)=[CH:5][CH:4]=1)#[N:2].[ClH:31]>O>[ClH:31].[C:1]([C:3]1[CH:4]=[CH:5][C:6]([CH2:9][CH2:10][N:11]2[CH2:16][CH2:15][C:14]([CH2:18][N:19]([CH3:30])[C:20]3[CH:28]=[CH:27][C:23]([C:24]([OH:26])=[O:25])=[CH:22][C:21]=3[CH3:29])([OH:17])[CH2:13][CH2:12]2)=[CH:7][CH:8]=1)#[N:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound (310 mg) obtained in Example 3 was suspended in water (15 mL) and was dissolved therein by addition of 1 N hydrochloric acid (3.0 mL) with heating under reflux. After cooling, the solvent was removed under reduced pressure, the residue was pulverized, was dried under reduced pressure to yield the titled compound (274 mg) as a powder.
Workup
- dissolutionwas dissolved
- temperaturewith heating
- temperatureunder reflux
- temperatureAfter cooling
- customthe solvent was removed under reduced pressure
- customwas dried under reduced pressure
Sources & evidence
- ORD record
- ord-893b2729303f4054a36a237dba7d7ee5
- Source dataset
- uspto-grants-2009_02
- Patent number
- US07494987B2
Reaction notes
Loading…