HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127099Generated: November 2, 2026
Hydrochloric Acid → HCID 131712110, compound
https://huagongshe.com/reaction/127099
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Agr 307 | HCID 73233 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 20130112 | HCID 20130112 | — |
| Reactant | HCID 70572016 | HCID 70572016 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131712110 | HCID 131712110 | — |
Reaction Steps
A mixture of 2-(2-aminothiazol-4-ylmethyl)isothiourea (1.57 g.) and 1 N sodium hydroxide (24 ml.) was stirred for 15 minutes at room temperature, and then the mixture was adjusted to pH 9 with 1 N hydrochloric acid (12 ml.). Thus obtained solution containing 2-aminothiazol-4-ylmethanethiol was dropwise added to a mixture of 3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-7-bromoacetamido-3-cephem-4-carboxylic acid (2.16 g.), sodium bicarbonate (0.67 g.), water (33 ml.) and ethanol (33 ml.) over 15 minutes at room temperature with stirring. The mixture was stirred for 1 hour at room temperature, and it was adjusted to pH 4 with 1 N hydrochloric acid. The mixture was allowed to stand for overnight in a refrigerator, and the precipitates were collected by filtration, washed with a small amount of water and then dried to give powder of 3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-7-(2-aminothiazol-4-yl)methylthioacetamido-3-cephem-4-carboxylic acid (0.7 g.), mp 180° to 250° C. (dec.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04254260 |
|---|
| Source dataset | uspto-grants-1981_03 |
|---|
| ORD ID | ord-74f9edd6201f4b688b517b008f72ced3 |
|---|
| Source note | uspto-grants-1981_03 |
|---|