HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364533Generated: October 26, 2026
N,N-Dimethylaniline → 4-Nitrobenzyl 7-amino-3-hydroxy-3-cephem-4-carboxylate
https://huagongshe.com/reaction/364533
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | (6S)-4-Nitrobenzyl 3-hydroxy-8-oxo-7-(N-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | HCID 67685788 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-Nitrobenzyl 7-amino-3-hydroxy-3-cephem-4-carboxylate | HCID 68123235 | 69.5% |
Reaction Steps
Triethylamine (2.37 g.), dimethylaniline (7.12 g.) and trimethylsilyl chloride (3.93 g.) were added to a stirred suspension of 4-nitrobenzyl 7-(2-phenylacetamido)-3-hydroxy-3-cephem-4-carboxylate (10 g.) in methylene chloride (200 ml.) in turn, and the solution was stirred at room temperature for an hour. Phosphorus pentachloride (4.88 g.) was added to the solution at -30° to -25° C. and stirred at -25° to -20° C. for 3 hours. Methanol (42 ml.) was added to the solution at -25° to -20° C., and stirred for an hour. To the solution was added water (35 ml.) at -25° to -20° C., and the solution was stirred at room temperature. The precipitates were collected by filtration, washed with methylene chloride and diethyl ether in turn, and dried to give 4-nitrobenzyl 7-amino-3-hydroxy-3-cephem-4-carboxylate (5.2 g.), mp 148° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04604456 |
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| Source dataset | uspto-grants-1986_08 |
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| ORD ID | ord-1f60fe6fafe34dc1973aee86cdaaeb9d |
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| Source note | uspto-grants-1986_08 |
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