Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178477301 | HCID 178477301 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178477300 | HCID 178477300 | 90.7% |
Reaction Steps
To a solution of 7β-[(Z)-2-(2-t-butoxycarbonylaminothiazol -4-yl)-2-trityloxyiminoacetylamino]-3-(1-methyl-1,2,4-triazol-3-ylthiomethylthio)-3-cephem-4-carboxylic acid diphenylmethyl ester 1-oxide (1.78 g : 1.69 mMol.) in dimethylformamide (15 ml) at -20° C. is added phosphorus trichloride (0.42 ml : 4.18 mMol.), and the mixture is stirred at the same temperature for 20 minutes. The reaction mixture is poured into two layers of cold aqueous sodium hydrogen carbonate and ethyl acetate. The organic layer is taken, washed with water and brine, dried over sodium sulfate, and concentrated. The residue is purified by silica gel chromatography (toluene : ethyl acetate=2: 1) to give 7β-[(Z)-2- (2-t-butoxycarbonylaminothiazol-4-yl) -2-trityloxyiminoacetamido]-3-(1- methyl-1,2,4-triazol-3-ylthiomethylthio) -3-cephem-4-carboxylic acid diphenylmethyl ester (1.59 g) as brown foam. Yield : 91%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05214037 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-46edc95796b44a0c93415e317bd9fb51 |
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| Source note | uspto-grants-1993_05 |
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