HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591264Generated: October 31, 2026
Dimethylformamide → HCID 141560924, compound
https://huagongshe.com/reaction/1591264
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 14864656 | HCID 14864656 | — |
| Reactant | HCID 88467418 | HCID 88467418 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 141560924 | HCID 141560924 | 86% |
Reaction Steps
A mixture of diphenylmethyl 7-amino-3-(3,4-dioxo-2-methyl-1-cyclobutenyl)-3-cephem-4-carboxylate (100 mg, 0.217 mmol) and 1-[2-(2-aminothiazol-4-yl)-(Z)-2-methoxyiminoacetyl]-4-methyltetrazole-5-thione (65 mg, 0.217 mmol) in tetrahydrofuran (1 mL) was stirred at 5° C. for 0.25 hr and then for 1 hr at 22° C. when N,N-dimethylformamide (0.05 mL) was added. The solution was diluted with ethyl acetate. The solution was sequentially washed with dilute aqueous NaHCO3 (2×), H2O, and saturated NaCl and then was dried over Na2SO4. Removal of the solvent left a yellow solid which was chromatographed on SiO2 (6 g) with methylene chloride/2-propanol (96:4) to afford the title compound (120 mg, 86% yield) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05206360 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-6c42440dab674c0390165e8e726e71c5 |
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| Source note | uspto-grants-1993_04 |
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