Hydrochloric Acid → HCID 19046249, compound
Reaction equation
[N:1]1([CH2:13][CH2:14][NH:15][C:16](=[O:18])[CH3:17])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]3[O:12][CH2:11][CH2:10][C:8]3=2)[CH2:3][CH2:2]1.[ClH:19]>C(OCC)(=O)C>[ClH:19].[N:1]1([CH2:13][CH2:14][NH:15][C:16](=[O:18])[CH3:17])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]3[O:12][CH2:11][CH2:10][C:8]3=2)[CH2:3][CH2:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound of Example 3 (334 mg) was dissolved in ethyl acetate (20 ml) and was treated with ethereal HCl (1.35 ml). This was stirred at room temperature for 2 h and then the solvent was evaporated to give the title compound as a pale green powder (383 mg), m.p. 152°-154° C.
Workup
- customthe solvent was evaporated
Sources & evidence
- ORD record
- ord-6f742d84ff9d4b8e8717082162d207dc
- Source dataset
- uspto-grants-1997_05
- Patent number
- US05633276
Reaction notes
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