HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154813Generated: October 28, 2026
Thiourea → 7-[2-(2-Amino-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/1154813
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 7-(2-Methoxyimino-3-oxo-bromobutyramido)-3-cephem-4-carboxylic acid | HCID 131712504 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-[2-(2-Amino-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid | HCID 131712444 | 20.2% |
Reaction Steps
Thiourea (8.4 mg.) was added to a solution of 7-(2-methoxyimino-3-oxo-4-bromobutyramido)-3-cephem-4-carboxylic acid (syn isomer, 42 mg.) in ethanol (6 ml.) and stirred at room temperature for an hour and at 50° C. for 30 minutes. After removing ethanol from the reaction mixture in vacuo, water (5 ml.) was added to the residue and adjusted to pH 4.0 with 6 N-hydrochloric acid. The precipitates were collected by filtration and dried to give 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid (syn isomer, 8 mg.). The filtrate was subjected to column chromatography on nonionic, adsorption resin "Diaion HP-20" (trademark: manufactured by Mitsubishi Chemical Industries Ltd., 5 ml.), washed with chilled water (5 ml.) and eluted with 20% aqueous isopropyl alcohol. The eluate was adjusted to pH 6.5 with 1 N aqueous sodium hydroxide under ice-cooling, and concentrated in vacuo. The residue was lyophilized to give sodium 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylate (syn isomer, 15 mg.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04298529 |
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| Source dataset | uspto-grants-1981_11 |
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| ORD ID | ord-712219320ebc443fa7f5d53a334d3920 |
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| Source note | uspto-grants-1981_11 |
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