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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64748Generated: October 29, 2026

Pyridine → HCID 88601078, compound

https://huagongshe.com/reaction/64748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiisopropyl EtherHCID 7914—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantBenzhydryl 7-phenylacetamido-3-(2,2-dibromovinyl)-2-cephem-4-carboxylateHCID 88600993—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 88601078HCID 8860107897.8%

Reaction Steps

To a suspension of phosphorus pentachloride (13.74 g) in dichloromethane (150 ml) was dropwise added pyridine (5.34 ml) at -15° to -10° C. under stirring which was continued at the same temperature for 30 minutes. To the above mixture was added benzhydryl 7-phenylacetoamido-3-(2,2-dibromovinyl)-2-cephem-4-carboxylate (29.4 g) at -5° C. After the reaction mixture was stirred at -5° for 1.5 hours, methanol (26.62 ml) was dropwise added to the reaction mixture under cooling at -20° and the mixture was stirred at -20° C. to -5° C. for 1.5 hours. Then water (30 ml) was added to the reaction mixture under ice-cooling. After the reaction mixture was stirred for an hour at the same temperature, diisopropylether (100 ml) was added to the reaction mixture at 0° C. The resultant precipitates were collected by filtration and washed in turn with water and diisopropyl ether to give benzhydryl 7-amino-3-(2,2-dibromovinyl)-2-cephem-4-carboxylate hydrochloride (25.23 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609730
Source datasetuspto-grants-1986_09
ORD IDord-f5ff54d63f264e73a94f49d38810e941
Source noteuspto-grants-1986_09