HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → 7-Methylsulfonylacetamido-3-cephem-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-Methanesulfonylacetic acid | HCID 3732841 | — |
| Reactant | Benzhydryl 7-amino-3-cephem-4-carboxylate | HCID 12098365 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Methylsulfonylacetamido-3-cephem-4-carboxylic acid | HCID 68147876 | — |
Reaction Steps
A solution of benzhydryl 7-amino-3-cephem-4-carboxylate (0.78 g, 2 mmol), methylsulfonylacetic acid (0.27 g, 2 mmol), and dicyclohexylcarbodiimide (0.4 g, 2 mmol) in dry tetrahydrofuran (15 ml) is stirred at room temperature overnight. The precipitate is collected and washed with tetrahydrofuran and the combined filtrate and washings are evaporated iin vacuo. The residue is treated with a cold solution of trifluoroacetic acid (10 ml) and anisole (0.5 g) for 15 minutes and then concentrated in vacuo. The residue is dissolved in ethyl acetate and treated with 5% MaHCO3. The aqueous phase is adjusted to pH 2 and the precipitated product is collected and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03948905 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-6f9c1126f3e04be3a8e42677e02165d6 |
| Source note | uspto-grants-1976_04 |