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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164685Generated: October 30, 2026

Hydrochloric Acid → HCID 131712387, compound

https://huagongshe.com/reaction/2164685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 131712380HCID 131712380—
SolventMethanolHCID 887—
ProductHCID 131712387HCID 13171238723.2%

Reaction Steps

To a suspension of 7-[2-{N-(3-pyridyl)carbamoylmethoxyimino}-2-(2-formamidothiazol-4-yl)acetamido]-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (2.7 g.) in methanol (40 ml.) was added conc. hydrochloric acid (1.09 ml.) with stirring at room temperature followed by stirring for 2 hours at the same temperature. The reaction mixture was separated by decantation into two groups, that is, a methanol layer and viscous precipitates. The methanol layer was treated with activated charcoal and concentrated and then the residue was dissolved in water. After the solution was adjusted to pH 3 to 4 with an aqueous solution of sodium bicarbonate, the precipitates are collected by filtration to give a powder of the title compound (0.6 g.). On the other hand, the viscous precipitates were dissolved in a mixture of methanol conc. hydrochloric acid and water and the solution was stirred for an hour at room temperature, treated with activated charcoal and then concentrated. The residue was dissolved in water and thereto was added an aqueous solution of sodium bicarbonate under cooling whereby the pH was adjusted to 3 to 4. The precipitates were collected by filtration to give a powder of the title compound (1.0 g.). Total

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04506076
Source datasetuspto-grants-1985_03
ORD IDord-b05dd5f0c03c4790b0db387545c10e10
Source noteuspto-grants-1985_03