HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412737Generated: November 1, 2026
N,N-Dimethylaniline → 7-amino-3-(1-allyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/2412737
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Glycol monoethyl ether | HCID 8076 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | HCID 131712576 | HCID 131712576 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-amino-3-(1-allyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid | HCID 70432653 | 59.5% |
Reaction Steps
N,N-Dimethylaniline (18.2 ml) was added to a mixture of ammonium 7-(5-amino-5-carboxyvaleramido)-3-(1-allyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylate (10.0 g), trimethylsilyl chloride (20.9 ml) and methylene chloride (75 ml), and the mixture was stirred under reflux for 2.5 hours. Phosphorus pentachloride (5.83 g) was added thereto at -30° to -35° C. and the mixture was stirred for 2 hours at the same temperature. 2-Ethoxyethanol (38 ml) was added dropwise thereto at the same temperature and the mixture was stirred for 1 hour at the same temperature. Water (80 ml) was added thereto at -5° to -10° C. over 10 minutes and the resulting mixture was stirred for 5 minutes at the same temperature. The aqueous layer was separated and adjusted to pH 4.2 with 28% aqueous solution of ammonia. Precipitates were collected by filtration, washed with 70% aqueous acetone (40 ml) and methanol (40 ml), and dried to give 7-amino-3-(1-allyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (4.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04493833 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-522f04d62cee416584dabf85dbe939f5 |
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| Source note | uspto-grants-1985_01 |
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