Sodium Hydroxide → HCID 67434998, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][N:9]2[C:13]3[CH:14]([C:17](C(OCC)=O)(C(OCC)=O)[C:18]([O:20]CC)=[O:19])[CH2:15][CH2:16][C:12]=3[N:11]=[C:10]2[CH:33]([CH3:35])[CH3:34])=[CH:4][CH:3]=1.[OH-].[Na+]>CO>[NH3:9].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][N:9]2[C:13]3[CH:14]([CH2:17][C:18]([OH:20])=[O:19])[CH2:15][CH2:16][C:12]=3[N:11]=[C:10]2[CH:33]([CH3:35])[CH3:34])=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Intermediate 20 (50 mg) was dissolved in methanol (3 ml) and the resulting soln. was treated with sodium hydroxide, 3M aq. (1 ml). The resulting suspension was heated to reflux for 4 hr. The reaction mixture was allowed to cool and concentrated in vacuo. The crude residue was taken up in acetic acid (10 ml) and heated to reflux for 2 h.
Workup
- temperatureThe resulting suspension was heated
- temperatureto reflux for 4 hr
- temperatureto cool
- concentrationconcentrated in vacuo
- temperatureheated
- temperatureto reflux for 2 h.
Sources & evidence
- ORD record
- ord-9e691efde5e7405687032ec42ac446b6
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08399444B2
Reaction notes
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