Triethylamine → (6R,7R)-3-(carbamoyloxymethyl)-7-[[2-(2-furanyl)-2-methoxyimino-1-oxoethyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

Participants

Reaction Steps

N,N-Dimethylacetamide (1.5 ml) was added to a solution of phosphorus pentachloride (750mg, 3.6mmole) in anhydrous dichloromethane (15ml) cooled to -10°. After 10 minutes, 2-(fur-2-yl)-2-methoxyiminoacetic acid (syn isomer) (612mg, 3.6mmole) was added to the resulting suspension, which soon became a clear solution and was stirred at -10° for 15 minutes. Ice (3g) was added and after 10 minutes the layers were allowed to separate in a dropping funnel. The organic phase was slowly (over 5 minutes) run into a cooled (-10°) solution of (6R,7R)-7-amino-3-chloroacetylcarbamoyloxymethylceph-3-em-4-carboxylic acid (1.05g, 3mmole) in dichloromethane (15ml) containing triethylamine (0.9ml, 6.5mmole). Methanol (1ml) was added after 40 minutes, and 5 minutes later the reaction mixture was extracted twice with 3% w/v aqueous sodium bicarbonate solution (150ml). The aqueous extract was washed with ethyl acetate (25ml) and left at 20° for 4 hours. The solution was washed twice with ethyl acetate, acidified with 2N-hydrochloric acid, and extracted 3 times with ethyl acetate. The combined organic layers were dried over magnesium sulphate, decolourised with activated charcoal, and evaporated in vacuo to give a pale-yellow solid (1.15g, 87%). This was washed with diethyl ether and filtered off to give the title compound (0.91g,71%); λmaxpH6 274nm (ε17,300). The IR and NMR spectra of the product agreed with those of an authentic sample.

Provenance & Evidence