Ethanol → sodium (5R,6S)-2-amino-6-[(R)-1-hydoxyethyl]carbapen-2-em-3-carboxylate
Reaction equation
[N:1]([C:4]1[CH2:5][C@@H:6]2[C@@H:23]([C@H:24]([OH:26])[CH3:25])[C:22](=[O:27])[N:7]2[C:8]=1[C:9]([O:11]CC1C=CC([N+]([O-])=O)=CC=1)=[O:10])=[N+]=[N-].O1CCCC1.C(O)C.C(=O)(O)[O-].[Na+:40]>[Pd].O>[NH2:1][C:4]1[CH2:5][C@@H:6]2[C@@H:23]([C@H:24]([OH:26])[CH3:25])[C:22](=[O:27])[N:7]2[C:8]=1[C:9]([O-:11])=[O:10].[Na+:40]Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of p-nitrobenzyl (5R,6S)-2-azido-6-[(R)-1-hydroxyethyl]carbapen-2-em-3-carboxylate (75 mg, 0.2 mmol), tetrahydrofuran (14 ml), ethanol (14 ml), deionized water (11 ml) containing sodium bicarbonate (16.8 mg, 0.2 mmol), and 10% palladium on carbon (75 mg) is shaken under hydrogen (45 psi) at ambient temperature for 2 hours. The mixture is filtered through a celite pad to remove the catalyst which is washed with water. The combined filtrate and wash is extracted with three portions of diethyl ether, concentrated under vacuum to about 10 ml volume, and lyophilized to afford sodium (5R,6S)-2-amino-6-[(R)-1-hydroxyethyl]carbapen-2-em-3-carboxylate.
Workup
- filtrationThe mixture is filtered through a celite pad
- customto remove the catalyst which
- washis washed with water
- washThe combined filtrate and wash
- extractionis extracted with three portions of diethyl ether
- concentrationconcentrated under vacuum to about 10 ml volume
Sources & evidence
- ORD record
- ord-5d179fb91de04cb19b3f8ef86496ab68
- Source dataset
- uspto-grants-1990_01
- Patent number
- US04892869
Reaction notes
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