Hydrochloric Acid → HCID 68508069, compound
Reaction equation
[Cl:1][C:2]1[CH:32]=[CH:31][C:5]([CH2:6][CH:7]([C:15]([NH:17][S:18]([C:21]2[CH:30]=[CH:29][C:28]3[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=3)[CH:22]=2)(=[O:20])=[O:19])=[O:16])[C:8](N(CC)CC)=[O:9])=[CH:4][CH:3]=1.Cl.C(OCC)(=[O:36])C>>[Cl:1][C:2]1[CH:32]=[CH:31][C:5]([CH2:6][CH:7]([C:15]([NH:17][S:18]([C:21]2[CH:30]=[CH:29][C:28]3[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=3)[CH:22]=2)(=[O:20])=[O:19])=[O:16])[C:8]([OH:36])=[O:9])=[CH:4][CH:3]=1Participants
4
Procedure
To the compound (2.10 g) obtained in Example 110 (4) were added 0.5 mol/L hydrochloric acid (40 ml) and ethyl acetate (80 mL), and the organic layer was collected by partitioning and washed with brine. The organic layer was concentrated under reduced pressure to give the title compound (1.90 g) as a white solid.
Workup
- customthe organic layer was collected
- customby partitioning
- washwashed with brine
- concentrationThe organic layer was concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-0c6c56b6d5784a5181f83d5b4ab8d006
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08461209B2
Reaction notes
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