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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195548Generated: October 31, 2026

Sodium Iodide → Phthalid-3-yl 7-[2(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate

https://huagongshe.com/reaction/1195548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantEthyl AcetateHCID 8857—
Reactant1(3H)-Isobenzofuranone, 3-bromo-HCID 96218—
ReactantSodium 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylateHCID 131713178—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductPhthalid-3-yl 7-[2(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylateHCID 131713182—

Reaction Steps

To a solution of sodium 7[2-(2-aminothiazol-4-yl) -2-methoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate (syn isomer(2.16 g) in N,N-dimethylformamide (20 ml) were added 3-bromophthalide (1.3 g) and sodium iodide (1.35 g), and the mixture was stirred at ambient temperature for 40 minutes. Thereto were added ethyl acetate (100 ml) and water (50 ml), and the separated ethyl acetate layer was washed with a saturated aqueous solution of sodium bicarbonate and an aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. After removal of the solvent, the residue (2.6 g) was chromatographed on silica gel (50 g) using a mixture of benzene and ethyl acetate as an eluent. The fractions containing the desired compound were collected and evaporated to give phthalid-3-yl 7-[2-(2-aminothiazol -4-yl)-2-methoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate (syn isomer) (1.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110921
Source datasetuspto-grants-1992_05
ORD IDord-7f6dd076737842928377e368cec1a7bc
Source noteuspto-grants-1992_05