Hydrochloric Acid → HCID 11525216, compound
Reaction equation
[CH3:1][C:2]1[C:6]([CH2:7][O:8][C:9]2[CH:14]=[CH:13][C:12]([CH2:15][C@H:16]([NH:21][C:22]3[S:23][CH:24]=[C:25]([C:27]4[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=4)[N:26]=3)[C:17]([O:19]C)=[O:18])=[CH:11][CH:10]=2)=[C:5]([CH3:33])[O:4][N:3]=1.[Li+].[OH-].Cl.O>C1COCC1.CO.O>[CH3:1][C:2]1[C:6]([CH2:7][O:8][C:9]2[CH:10]=[CH:11][C:12]([CH2:15][C@H:16]([NH:21][C:22]3[S:23][CH:24]=[C:25]([C:27]4[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=4)[N:26]=3)[C:17]([OH:19])=[O:18])=[CH:13][CH:14]=2)=[C:5]([CH3:33])[O:4][N:3]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
The crude product from Step B was dissolved in a THF/MeOH/H2O mixture (6:0.1:1; 2 ml). Aqueous 1M LiOH solution (1.6 ml) was added and the mixture was stirred for 3 days at room temperature. Then the reaction mixture was neutralized with 1M HCl, a small amount of water was added, and the mixture extracted with ethyl acetate. The solvent was evaporated.
Workup
- extractionthe mixture extracted with ethyl acetate
- customThe solvent was evaporated
Sources & evidence
- ORD record
- ord-094fb7f562ae4c5e951cf248d4778e1f
- Source dataset
- uspto-grants-2007_12
- Patent number
- US07309791B2
Reaction notes
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