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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681450Generated: November 3, 2026

Methanol → Benzhydryl 7-Amino-3-chloromethyl-3-cephem-4-carboxylate

https://huagongshe.com/reaction/1681450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPyridineHCID 1049—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantBenzhydryl 3-hydroxymethyl-7-phenylacetamido-3-cephem-4-carboxylateHCID 13339796—
SolventDichloromethaneHCID 6344—
ProductBenzhydryl 7-Amino-3-chloromethyl-3-cephem-4-carboxylateHCID 13239626—

Reaction Conditions

Temperature-20 °C

Reaction Steps

19.64 ml (0.242 mol) of pyridine are added to a suspension of 50 g (0.0972 mol) of benzhydryl 7-phenylacetamido-3-hydroxymethyl-3-cephem-4-carboxylate in 500 ml of methylene chloride at room temperature. After cooling to -20° C., 40.48 g (0.0972 mol) of phosphorus pentachloride are added and the mixture is stirred at -20° C. for 5 minutes. The mixture is warmed to 0° C. with an icebath and stirred for 10 minutes, and is then warmed to 15° C. with a waterbath and stirred for 1 hour. Thereafter, the mixture is cooled to -70° C. and 720 ml of cold methanol are quickly added The mixture is then stirred at -70° C. for 5 minutes, at 0° C. for 10 minutes and at +15° C. for 25 minutes. The solution is subsequently concentrated to a high degree in vacuo and 1,400 ml of saturated sodium bicarbonate solution are added. The solution is extracted three times with methylene chloride and the organic phase is dried with sodium sulphate and concentrated in vacuo. The crude product is chromatographed on 500 g of silica gel 60 (0.04-0.063 mm) with methylene chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05171854
Source datasetuspto-grants-1992_12
ORD IDord-f7fa88ce9c704db4b8df998686534428
Source noteuspto-grants-1992_12