Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Methylthiourea | HCID 2723704 | — |
| Reactant | HCID 178501866 | HCID 178501866 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178482390 | HCID 178482390 | 69% |
Reaction Steps
A mixture of 7-[4-chloro-2-(methoxycarbonylmethoxyimino)-3-oxobutyramido]-3-methylthio-3-cephem-4-carboxylic acid (syn isomer) (4.3 g), N-methylthiourea (1.8 g) and sodium acetate (4.1 g) in water (20 ml) and tetrahydrofuran (40 ml) was stirred at 38° to 42° C. for 2.5 hours. Water (50 ml) was added to the reaction mixture and the resultant solution was washed with ethyl acetate. The separated aqueous layer was acidified to pH 2.3 with 10% hydrochloric acid and then extracted with ethyl acetate. The ethyl acetate layer was washed with brine and dried over magnesium sulfate. The solution was evaporated and the residue was triturated with ether to give 7-[2-(2-methylaminothiazol-4-yl)-2-(methoxycarbonylmethoxyimino)acetamido]-3-methylthio-3-cephem-4-carboxylic acid (syn isomer) (3.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04452851 |
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| Source dataset | uspto-grants-1984_06 |
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| ORD ID | ord-c6ea36947b054a5ebe705951833f3166 |
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| Source note | uspto-grants-1984_06 |
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