Ethanol → sodium (5R,6S)-2-amino-6-[(R)-1-hydoxyethyl]carbapen-2-em-3-carboxylate

HRID 2231705Notes

Reaction equation

HRID 2231705 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

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

  1. filtrationThe mixture is filtered through a celite pad
  2. customto remove the catalyst which
  3. washis washed with water
  4. washThe combined filtrate and wash
  5. extractionis extracted with three portions of diethyl ether
  6. concentrationconcentrated under vacuum to about 10 ml volume

Sources & evidence

ORD record
ord-65763a5898ba40a7988aae92cba72154
Source dataset
uspto-grants-1988_11
Patent number
US04783453

Reaction notes

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