HCID 86753214, compound → HCID 18665857, compound
Reaction equation
[CH2:1]([NH:5][S:6]([NH:9][C@@H:10]([CH2:16][NH:17]C(OC(C)(C)C)=O)[C:11]([O:13][CH2:14][CH3:15])=[O:12])(=[O:8])=[O:7])[CH2:2][CH2:3][CH3:4]>C(OCC)(=O)C>[CH2:1]([NH:5][S:6]([NH:9][C@@H:10]([CH2:16][NH2:17])[C:11]([O:13][CH2:14][CH3:15])=[O:12])(=[O:7])=[O:8])[CH2:2][CH2:3][CH3:4]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 9-2 (612 mg, 1.65 mmol) in ethyl acetate (50 ml) was cooled to -5° and anhydrous HCl was bubbled in for 30 min. The reaction was concentrated and the product isolated by filtration to give 9-3 as a white solid.
Workup
- customanhydrous HCl was bubbled in for 30 min
- concentrationThe reaction was concentrated
- customthe product isolated by filtration
Sources & evidence
- ORD record
- ord-ee56789f8e164366bf553197365c0992
- Source dataset
- uspto-grants-1998_10
- Patent number
- US05821241
Reaction notes
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