Hydrochloric Acid → HCID 22874920, compound
Reaction equation
[C:1]1([S:7]([NH:10][C@@H:11]([CH2:19][CH2:20][CH2:21][C:22]2[CH:27]=[CH:26][C:25]([O:28][CH2:29][CH2:30][CH2:31][C:32]3[N:33]=[CH:34][N:35]([CH3:37])[CH:36]=3)=[CH:24][CH:23]=2)[C:12]([O:14]C(C)(C)C)=[O:13])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl>CCOC(C)=O>[C:1]1([S:7]([NH:10][C@@H:11]([CH2:19][CH2:20][CH2:21][C:22]2[CH:27]=[CH:26][C:25]([O:28][CH2:29][CH2:30][CH2:31][C:32]3[N:33]=[CH:34][N:35]([CH3:37])[CH:36]=3)=[CH:24][CH:23]=2)[C:12]([OH:14])=[O:13])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
A solution of 35-9 (0.055 g, 0.127 mmol) in EtOAc (1 mL) was cooled to -78° C., and saturated with HCl gas. The reaction was warmed to 0° C. for 1/2 hr, then concentrated and the residue chromatographed (20:1:1 EtOH/NH4OH/H2O) to give 35-10 as a white solid.
Workup
- concentrationconcentrated
- customthe residue chromatographed (20:1:1 EtOH/NH4OH/H2O)
Sources & evidence
- ORD record
- ord-f13616bb926a445fb43bc00081905cc0
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05648368
Reaction notes
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