Potassium Bicarbonate → HCID 18598138, compound

HRID 463370Notes

Reaction equation

HRID 463370 reaction equation
C(=O)(O)[O-].[K+].[H][H].[N+](C1C=CC(C[O:16][C:17]([C@@H:19]2[N:23]3[C:24](=[O:40])[C@@H:25]([NH:26]C(OCC4C=CC([N+]([O-])=O)=CC=4)=O)[C@H:22]3[S:21][C@:20]2([CH2:42][O:43][C:44](=[O:46])[NH2:45])[CH3:41])=[O:18])=CC=1)([O-])=O>[Pd].C(OCC)(=O)C>[NH2:26][C@@H:25]1[C:24](=[O:40])[N:23]2[C@@H:19]([C:17]([OH:18])=[O:16])[C@@:20]([CH2:42][O:43][C:44](=[O:46])[NH2:45])([CH3:41])[S:21][C@H:22]12

Participants

6

Procedure

A suspension of 10% palladium on charcoal (0.50 g) in ethyl acetate (25 ml) and aqueous potassium bicarbonate (0.4%, 22.5 ml, 0.10 g inorganics) was prehydrogenated at 50 psi hydrogen for 15 minutes. The suspension was charged under nitrogen with (2R,3S,5R,6R) 6-(4-nitrobenzyloxycarbonyl)amino-2-carbamoyloxymethyl-2-methylpenam-3-carboxylic acid p-nitrobenzyl ester (0.54 g, 0.9 mmol) and the whole was shaken at 50 psi hydrogen pressure for 1.2 hours. The mixture (pH 5.0) was centrifuged and the aqueous phase was washed with methylene chloride (2×15 ml), combined with a water back extract (10 ml), and concentrated to about a 2 ml volume. The rich aqueous phase was diluted with deuterium oxide (4 ml) frozen on dry-ice and lyophilized to give a light yellow solid (0.25 g; theory=0.25 g+inorganics 0.10 g) in 66% product yield; nmr 100 MHz (D2O) ppm 4.63 (1, d, J=4.0 Hz, C6 --H), 4.46 (1, s, C3 --H), C5 --H under HOD, 4.18 (1, d, J=11.5, 1/2 AB C2 --CHH--O), 4.01 (1, d, J=11.5, C2 --CHHO), and 1.53 (3, s, C2 --CH3).

Workup

  1. washthe aqueous phase was washed with methylene chloride (2×15 ml)
  2. extractionback extract (10 ml)
  3. concentrationconcentrated to about a 2 ml volume
  4. additionThe rich aqueous phase was diluted with deuterium oxide (4 ml)
  5. temperaturefrozen on dry-ice

Sources & evidence

ORD record
ord-080708e0de4d4aeda7828238cf35be4a
Source dataset
uspto-grants-1985_05
Patent number
US04518773

Reaction notes

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