Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905448Generated: October 26, 2026

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

https://huagongshe.com/reaction/905448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantEthyl AcetateHCID 8857—
ReactantIodomethyl hexanoateHCID 12775069—
ReactantHCID 88469259HCID 88469259—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHexanoyloxymethyl 7-[2-(2-aminothiazol-4-yl)acetamido]-3-vinyl-3-cephem-4-carboxylateHCID 8846933158.9%

Reaction Steps

To a solution of sodium 7-[2-(2-aminothiazol-4-yl)acetamido]-3-vinyl-3-cephem-4-carboxylate (2.0 g) in N,N-dimethylformamide (20 ml) were added iodomethyl hexanoate (3.4 g) and sodium iodide (3.1 g) in a stream of nitrogen, and the mixture was stirred at ambient temperature for 1.5 hours. After the reaction mixture was poured into a mixture of ethyl acetate (200 ml) and water (200 ml), the organic layer was separated out, washed with water and a saturated aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate, followed by treating with charcoal. The filtrate was concentrated, and thereto was added diisopropyl ether, followed by collecting the precipitated substance by filtration to obtain hexanoyloxymethyl 7-[2-(2-aminothiazol-4-yl)acetamido]-3-vinyl-3-cephem-4-carboxylate (1.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04423213
Source datasetuspto-grants-1983_12
ORD IDord-5d9aea0f17b54a5fb4cd78d911a5c2bb
Source noteuspto-grants-1983_12