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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893754Generated: October 29, 2026

Sodium Iodide → HCID 88496309, compound

https://huagongshe.com/reaction/893754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantHCID 178451068HCID 178451068—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
SolventSodium ThiosulfateHCID 24477—
ProductHCID 88496309HCID 88496309204.9%

Reaction Steps

To a solution of 7-[(Z)-2-(2-tritylaminothiazol-4-yl)-2-(1-tert-butoxycarbonyl-1-methylethoxyimino)acetamido]-3-[(Z)-3-chloro-1-propen-1-yl]-3-cephem-4-carboxylate (IXa) (1.23 g, 1.24 mmole) in acetone (5 ml) was added a solution of sodium iodide (560 mg, 3.72 mmol) in acetone (7 ml). The mixture was stirred at room temperature for 1.5 hour, and diluted with ethyl acetate (150 ml) and aqueous sodium thiosulfate solution. The organic layer was separated, dried over magnesium sulfate, and concentrated to give 1.38 g of diphenylmethyl 7-[(Z)-2-(2-tritylaminothiazol-4-yl)-2-(1-tert-butoxycarbonyl-1-methylethoxyimino)acetamido]-3-[(E)-3-iodo-1-propen-1-yl]-3-cephem-4-carboxylate (Xa) (see also Example 23 below) as an amorphous powder. Compound Xa was dissolved in ether (50 ml). The insoluble was filtered off and the filtrate was chilled in an ice-water bath, and was treated with a solution of 5,6-diacetoxy-2-methyl-2-isoindoline (600 mg, 2.4 mmol) in ether (50 ml). The mixture was stirred over 30 min, and the precipitate was collected by filtration to obtain 446 mg (27% yield) of the title iodide as a tan powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05126336
Source datasetuspto-grants-1992_06
ORD IDord-e8abb457dbb64227be4cb96527876848
Source noteuspto-grants-1992_06