HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607945Generated: October 30, 2026
Chlorotrimethylsilane → 7-Amino-3-(1-methyl-1-pyrrolidinio)methyl-3-cephem-4-carboxylate dihydrochloride
https://huagongshe.com/reaction/1607945
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 7-Benzoylamino-3-(1-methyl-1-pyrrolidinio)methyl-3-cephem-4-carboxylate | HCID 131716125 | — |
| Solvent | N,N-Dimethylaniline | HCID 949 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Isobutanol | HCID 6560 | — |
| Product | 7-Amino-3-(1-methyl-1-pyrrolidinio)methyl-3-cephem-4-carboxylate dihydrochloride | HCID 131716127 | — |
Reaction Steps
To a suspension of 7-benzoylamino-3-(1-methyl-1-pyrrolidinio)methyl-3-cephem-4-carboxylate (15 g) in a mixture of dichloromethane (300 ml) and N,N-dimethylaniline (41.7 g) was added dropwise trimethylsilyl chloride (31.2 g) at 5° C. After being stirred for 1 hour at 5°-10° C., the mixture was cooled up to -30° C. and then phosphorus pentachloride (11.9 g), was added thereto. After the mixture was stirred for 1 hour at -20°~-30° C., a mixture of isobutyl alcohol (21.2 g) and 1,3-propanediol (21.8 g) is dichloromethane (150 ml) cooled at -30° C. was added to the reaction mixture. The mixture was stirred for 1 day at room temperature to give a residue, which was collected by filtration, washed with dichloromethane, acetone and diisopropyl ether successively and dried over phosphorus pentoxide to give 7-amino-3-(1-methyl-1-pyrrolidinio)methyl-3-cephem-4-carboxylate dihydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04868174 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-886c498e8528474eb7fca18e84571504 |
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| Source note | uspto-grants-1989_09 |
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