Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 14608913 | HCID 14608913 | — |
| Reactant | HCID 178418395 | HCID 178418395 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15661276 | HCID 15661276 | — |
Reaction Steps
To a solution of 2-mercaptobenzothiazole (0.26 g. 1.54 mmol) in dry tetrahydrofuran (5.0 ml) at -78° C. was added sodium hydride (98%) (0.0369 g. 1.54 mmol). followed by diphenylmethyl 7-phenoxyacetamido-3-(trifluoromethylsulfonyloxy)-3-cephem-4-carboxylate (1.0 gm, 1.54 mmol). The reaction was warmed up to -20° C. and stirred for 16 hours before quenching in 0.5 N solution of hydrochloric acid (5 ml). The aqueous layer was extracted with dichloromethane (3×5 ml), dried (magnesium sulfate) and evaporated in vacuo to give the title compound as an oil which was purified by flash chromatography (silica, 40% ethylacetate in haxanes); yield isolated 0.7 g (70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05043439 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-6bf5135e5bee404083b1f8c66fcc3097 |
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| Source note | uspto-grants-1991_08 |
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