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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731696Generated: October 31, 2026

Hydrochloric Acid → HCID 131714956, compound

https://huagongshe.com/reaction/1731696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 131714952HCID 131714952—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 131714956HCID 13171495690.3%

Reaction Conditions

Temperature35 °C

Reaction Steps

To a suspension of benzhydryl 7-[2-(2-formamidothiazol-4-yl)-2-methoxyiminoacetamido]-3-[(Z)-2-(3-pyridyl)vinylthiomethyl]-3-cephem-4-carboxylate (syn isomer) (1.21 g) in methanol (24 ml) was added conc. hydrochloric acid (0.52 ml) at ambient temperature. The mixture was stirred for 1.5 hours at 35° C. The mixture was concentrated in vacuo to give a residue, which was dissolved in a mixture of ethyl acetate and water. The mixture was adjusted to pH 7 with an aqueous solution of sodium bicarbonate. The separated organic layer was washed with water and a saturated aqueous solution of sodium chloride in turn, dried over magnesium sulfate and concentrated in vacuo, and the residue was triturated in diisopropyl ether to give benzhydryl 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-[(Z)-2-(3-pyridyl)vinylthiomethyl]-3-cephem-4-carboxylate (syn isomer) (1.05 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04622318
Source datasetuspto-grants-1986_11
ORD IDord-6db886f78800418dbb05bec73b189b1b
Source noteuspto-grants-1986_11