Hydrochloric Acid → HCID 178504992, compound
Reaction equation
[CH3:1][S:2]([NH:5][C:6]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:7]=1[CH2:8][CH2:9][CH2:10][CH:11]2[C:16]1[N:17]=[CH:18][N:19](C(OC(C)(C)C)=O)[CH:20]=1)(=[O:4])=[O:3].Cl>CO>[NH:19]1[CH:20]=[C:16]([C@@H:11]2[CH2:10][CH2:9][CH2:8][C:7]3[C:6]([NH:5][S:2]([CH3:1])(=[O:4])=[O:3])=[CH:15][CH:14]=[CH:13][C:12]2=3)[N:17]=[CH:18]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of Example 9B (130 mg, 0.33 mmol) in methanol (10 mL) was treated with 1N HCl (5 mL), stirred for 1.5 hours, concentrated at 45° C., and dried under vacuum for 30 minutes. The residue was dissolved in methanol, filtered through cotton, concentrated and dried under vacuum for 3 hours to provide the desired compound.
Workup
- concentrationconcentrated at 45° C.
- customdried under vacuum for 30 minutes
- dissolutionThe residue was dissolved in methanol
- filtrationfiltered through cotton
- concentrationconcentrated
- customdried under vacuum for 3 hours
Sources & evidence
- ORD record
- ord-bf8522a48c54468b9dd3de812335e895
- Source dataset
- uspto-grants-2003_01
- Patent number
- US06503935B1
Reaction notes
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