HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543537Generated: October 25, 2026
Ammonia → 7-Amino-3-(1-methyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylicacid
https://huagongshe.com/reaction/543537
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Dacthal | HCID 2943 | — |
| Reactant | 7-Aminocephalosporanic acid | HCID 441328 | — |
| Reactant | Diphosphoryl tetrachloride | HCID 4432411 | — |
| Reactant | HCID 178482029 | HCID 178482029 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-Amino-3-(1-methyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylicacid | HCID 13020813 | 89.3% |
Reaction Steps
A 3.5 ml portion of acetonitrile was added to 0.570 g of dihydrate of 5-mercapto-1-methyl-1H-tetrazole sodium salt and 0.680 g of 7-ACA, and 1.64 g of diphosphoryl tetrachloride was added dropwise to the mixture under cooling over an external bath at -30° to -20° C., followed by adding 2.29 g of DCPA and rinsing with 0.5 ml of acetonitrile. The reaction solution was stirred at -5° to 0° C. for 5 minutes, warmed at 25° C., and stirred for 40 minutes to allow the reaction to proceed. The reaction solution was cooled and poured into ice-water, which was placed in a refrigerator overnight. The mixture was adjusted to pH 4.0 with 25% aqueous ammonia, and the resultant precipitate was recovered by filtration, washed with cold water and acetone successively and dried, thereby affording 0.732 g (89.3% of yield) of 7-amino-3-(1-methyl-1H-tetrazol-5 -yl)thiomethyl-3-cephem-4-carboxylic acid. The NMR values of the product were in accordance with those of the authentic sample.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04446318 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-724958eebe5b4a98a1c579349e172ea2 |
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| Source note | uspto-grants-1984_05 |
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