Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 21426457 | HCID 21426457 | — |
| Reactant | HCID 88826506 | HCID 88826506 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21426473 | HCID 21426473 | 10.3% |
Reaction Steps
5-Methoxy-2-thioxo-1,3,4-thiadiazoline (4.43 g.) and sodium bicarbonate (2.27 g.) in water (20 cc.) are added to the sodium salt of 3-acetoxymethyl-2-carboxy-8-oxo-7-[(1,3-dithiol-2-on-4-yl)-acetamido]-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene (12.2 g.) in a buffer (100 cc.) of pH 6.5. The mixture is heated under a nitrogen atmosphere to 50° C., for 5 hours. It is allowed to cool and treated with decolourising charcoal. Ethyl acetate (100 cc.) is added and the mixture is brought to pH 2.5 by adding 5 N hydrochloric acid while stirring. The organic phase is separated off and the aqueous phase is again extracted with ethyl acetate (160 cc.). The combined organic extracts are dried over sodium sulphate, treated with decolourising charcoal and then concentrated to dryness under reduced pressure (20 mm.Hg). A residue (11.5 g.) is obtained, and is triturated with acetonitrile (8 cc.) and isopropyl ether (8 cc.). A solid (2.4 g.) is filtered off and recrystallised from acetonitrile (375 cc.) and isopropyl ether (400 cc.) to give 2-carboxy-3-[(5-methoxy-1,3,4-thiadiazol-2-yl)-thiomethyl]-8-oxo-7-[(1,3-dithiol-2-on-4-yl)-acetamido]-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene (1.52 g.) m.p. 208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04034090 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-7faf45f3e3e04b16a7c6e9116fcacb06 |
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| Source note | uspto-grants-1977_07 |
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