Hydrochloric Acid → HCID 19045469, compound
Reaction equation
C(N[N:5]1[CH2:10][CH2:9][C:8]2([CH:15]([CH3:16])[C:14](=[O:17])[C:13]3[CH:18]=[C:19]([S:22]([CH3:25])(=[O:24])=[O:23])[CH:20]=[CH:21][C:12]=3[O:11]2)[CH2:7][CH2:6]1)(=O)C.[ClH:26]>CO>[ClH:26].[CH3:16][CH:15]1[C:8]2([CH2:7][CH2:6][NH:5][CH2:10][CH2:9]2)[O:11][C:12]2[CH:21]=[CH:20][C:19]([S:22]([CH3:25])(=[O:24])=[O:23])=[CH:18][C:13]=2[C:14]1=[O:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The product of Step B (0.5 g) in CH3OH (15 mL) and 6N HCl (15 mL) was heated at reflux for 10 hours. The reaction was concentrated to dryness and the residue flushed with ethanol (4 times) and then toluene to yield 0.5 g of the title compound.
Workup
- temperatureat reflux for 10 hours
- concentrationThe reaction was concentrated to dryness
- customthe residue flushed with ethanol (4 times)
Sources & evidence
- ORD record
- ord-f0fa6826a20f4f5cbf09a2936d2ca570
- Source dataset
- uspto-grants-1993_04
- Patent number
- US05206240
Reaction notes
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