Sodium Bicarbonate → HCID 70551266, compound

HRID 621108Notes

Reaction equation

HRID 621108 reaction equation
C([O:8][C:9]([CH:11]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[C:12]([NH:14][C@H:15]1[C@@H:18]([C:19]([O:21][CH3:22])=[O:20])[N:17]([S:23]([O-:26])(=[O:25])=[O:24])[C:16]1=[O:27])=[O:13])=[O:10])C1C=CC=CC=1.[Na+].C(=O)([O-])O.[Na+]>[Pd].C(O)C>[C:9]([CH:11]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[C:12]([NH:14][C@H:15]1[C@@H:18]([C:19]([O:21][CH3:22])=[O:20])[N:17]([S:23]([OH:26])(=[O:25])=[O:24])[C:16]1=[O:27])=[O:13])([OH:10])=[O:8]

Participants

5

Reactant 2

HCID 516892Sodium BicarbonateHCID 70390990HCID 70390990, compound

Product 1

HCID 70551266HCID 70551266, compound

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

To 6 ml of 80% ethanol are added 106 mg of sodium cis-3-(2-benzyloxycarbonyl-2-phenylacetamido)-4-methoxycarbonyl-2-oxoazetidine-1-sulfonate, 106 mg of 5% palladium-on-carbon and 16.8 mg of sodium hydrogen carbonate, and the mixture is vigorously stirred under hydrogen atmosphere for 3.5 hours at ambient temperature under atmosphere pressure. The reaction mixture is subjected to filtration, and the filtrate is concentrated under reduced pressure. The concentrate is purified by column chromatography on Amberlite XAD-II, followed by lyophilization to give cis-3-(2-carboxy-2-phenylacetamido)-4-methoxycarbonyl-1-sulfo-2-oxoazetidine.disodium salt as a mixture of diastereomers.

Workup

  1. filtrationThe reaction mixture is subjected to filtration
  2. concentrationthe filtrate is concentrated under reduced pressure
  3. customThe concentrate is purified by column chromatography on Amberlite XAD-II

Sources & evidence

ORD record
ord-708b2339583f429bb5006cad9fde1eb6
Source dataset
uspto-grants-1989_04
Patent number
US04822788

Reaction notes

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