HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127093Generated: October 26, 2026
Hydrochloric Acid → (2-Amino-1,3-thiazol-4-yl)acetic acid--hydrogen chloride (1/1)
https://huagongshe.com/reaction/127093
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (2-Amino-1,3-thiazol-4-yl)acetic acid | HCID 34665 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2-Amino-1,3-thiazol-4-yl)acetic acid--hydrogen chloride (1/1) | HCID 13017673 | — |
Reaction Steps
To a suspension of 2-aminothiazol-4-ylacetic acid (1.2 g.) in dried methylene chloride (75 ml.) was introduced dried hydrogen chloride gas under ice-cooling and stirring to produce 2-aminothiazol-4-ylacetic acid hydrochloride, and to the mixture was gradually added phosphorus pentachloride (4.0 g.) under ice-cooling and stirring and the mixture was stirred for 1 to 2 hours at room temperature. After removal of methylene chloride from the mixture, to the residue was added dried benzene and then the solvent was distilled off. The residue was dissolved in dried acetone (20 ml.), and the solution was dropwise added to a solution of 3-(1-allyl-1H-tetrazol-5-yl)thiomethyl-7-amino-3-cephem-4-carboxylic acid (1.8 g.) and sodium bicarbonate (2.1 g.) in a mixture of acetone (25 ml.) and water (25 ml.) under ice-cooling and stirring while the mixture was kept to pH 7.5 to 8.5 with triethylamine. The mixture was further stirred for 20 minutes, and acetone was removed at low temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04254260 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-9da45be07e294252aaa1a425d537134d |
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| Source note | uspto-grants-1981_03 |
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