HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569388Generated: October 25, 2026
Diisopropyl Ether → Hexanoyloxymethyl 7-[2-(2-aminothiazol-4-yl)-2-propargyloxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate
https://huagongshe.com/reaction/569388
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Iodomethyl hexanoate | HCID 12775069 | — |
| Reactant | HCID 131713172 | HCID 131713172 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Hexanoyloxymethyl 7-[2-(2-aminothiazol-4-yl)-2-propargyloxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate | HCID 131713171 | 75% |
Reaction Steps
To a solution of sodium 7-[2-(2-aminothiazol-4-yl)-2-propargyloxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate (syn isomer) (2 g) in N,N-dimethylformamide (20 ml) was added a solution of iodomethyl hexanoate (1.28 g) in N,N-dimethylformamide (4 ml) under ice-cooling, and the mixture was stirred at the same temperature for 15 minutes. To the reaction mixture was added ethyl acetate (80 ml), followed by washing twice with water, three times with 5% aqueous solution of sodium bicarbonate and twice with a saturated aqueous solution of sodium chloride. The resultant solution was dried over anhydrous magnesium sulfate and then evaporated to give a residue, which was pulverized with diisopropyl ether to obtain hexanoyloxymethyl 7-[2-(2-aminothiazol-4-yl)-2-propargyloxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate (syn isomer) (1.85 g), mp 98°-109° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04731443 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-f5c46bab41044a48980fa5a07cc7eeaa |
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| Source note | uspto-grants-1988_03 |
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