Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088037Generated: October 25, 2026

Sodium Iodide → HCID 178480376, compound

https://huagongshe.com/reaction/1088037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTetrahydrofuranHCID 8028—
Reactant1H-Pyrazole, 1-methyl-HCID 70255—
Reactant(6R,7R)-Benzhydryl 7-((tert-butoxycarbonyl)amino)-3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylateHCID 11756232—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 178480376HCID 178480376—

Reaction Steps

To a solution of sodium iodide (1.46 g) in acetone (5 ml) was added benzhydryl 7β-tert-butoxycarbonylamino-3-chloromethyl-3-cephem-4-carboxylate (5 g) at ambient temperature. The mixture was stirred at the same temperature for 10 minutes and N-methylpyrazole (5 ml) was added thereto. The resultant mixture was stirred at the same temperature for 24 hours and poured into a mixture of tetrahydrofuran (25 ml), ethyl acetate (25 ml) and water (25 ml). The separated organic layer was washed with brine, and dried over magnesium sulfate. The solution was evaporated in vacuo to give benzhydryl 7β-tert-butoxycarbonylamino-3-(2-methyl-1-pyrazolio)methyl-3-cephem-4-carboxylate iodide (6.45 g), the physical data of which were identical to those of the compound prepared in Preparation 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04960766
Source datasetuspto-grants-1990_10
ORD IDord-cfb8c45eb82741aa8f4a854fddd65083
Source noteuspto-grants-1990_10