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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463167Generated: November 2, 2026

p-Toluenesulfonic acid → 3-Acetoxymethyl-7-(imidazol-2-yl)aminoceph-3-em-4-carboxylic acid

https://huagongshe.com/reaction/1463167

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-Fluoro-1H-imidazoleHCID 559542—
Reactant3-Acetoxymethyl-7-amino-3cephem-4-carboxylic acidHCID 11346310—
SolventDimethylformamideHCID 6228—
Product3-Acetoxymethyl-7-(imidazol-2-yl)aminoceph-3-em-4-carboxylic acidHCID 7044549128.9%

Reaction Steps

A suspension of anhydrous toluene-p-sulphonic acid (0.74 g.) and 3-acetoxymethyl-7-aminoceph-3-em-4-carboxylic acid (1.17 g.) in dry DMF (17.5 ml.) was stirred for 15 minutes at room temperature to effect partial solution. One portion of 2-fluoroimidazole (0.74 g.) was then added and the mixture stirred at 90° for 2 hours. The solvent was evaporated at ambient temperature, 2% v/v aqueous HOAc (20 ml.) was added to the residue and the mixture was extracted with EtOAc (20 ml.). The aqueous layer was concentrated to 15 ml., filtered and the filtrate purified by preparative HPLC on Whatman "Partisil 10" using water/MeOH/HOAc 80:20:1 v/v/v as solvent. The product was further purified by trituration with acetone and washing with acetone and ether to give 3-acetoxymethyl-7-(imidazol-2-yl)aminoceph-3-em-4-carboxylic acid (0.42 g.) as a hydrated mixed acetate/toluene-p-sulphonate salt having m.p. >160° (decomp.) and the following n.m.r. in D2O: 2.28 (s, 3H); 3.58 (d, 1H); 3.89 (d, 1H); 4.92 (d, 1H); 5.13 (d, 1H); 5.42 (d, 1H); 5.70 (d, 1H); 7.08 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04463173
Source datasetuspto-grants-1984_07
ORD IDord-3a6bff0d8bef4b10aadc620caf7ac68a
Source noteuspto-grants-1984_07