HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27133Generated: October 29, 2026
Dimethylformamide → HCID 178513910, compound
https://huagongshe.com/reaction/27133
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-[(Trifluoromethyl)sulfanyl]acetic acid | HCID 3386253 | — |
| Reactant | 7-Amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid | HCID 178513909 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178513910 | HCID 178513910 | — |
Reaction Steps
A suspension of 3.85 g. (0.01 mol.) of 7-amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid in 50 ml. of dry dimethylformamide was treated with 2 ml. of triethylamine and the mixture was stirred for 15 minutes at 25°. The activated ester of trifluoromethylmercaptoacetic acid (2.57 g., 0.016 mol.) was added to the mixture and it was stirred an additional hour. The reaction mixture was evaporated to dryness and water and ethyl acetate were added to the residue. The layers were separated, ethyl acetate was added to the aqueous phase and it was acidified to pH 2.5 by addition of 6N hydrochloric acid. The mixture was filtered, the layers were separated and the aqueous phase was extracted with ethyl acetate. The extract was washed with water, dried (MgSO4) and evaporated to dryness to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04220644 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-2b641d84180448b3873fe599834e67dc |
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| Source note | uspto-grants-1980_09 |
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