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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905805Generated: November 2, 2026

Pyridine → Benzhydryl 7-amino-3-cephem-4-carboxylate

https://huagongshe.com/reaction/1905805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant3-Acetoxy-7beta-phenylacetylaminocepham-4-carboxylic acid diphenylmethyl esterHCID 13785482—
SolventDichloromethaneHCID 6344—
SolventIsobutanolHCID 6560—
ProductBenzhydryl 7-amino-3-cephem-4-carboxylateHCID 1209836560.8%

Reaction Steps

To a solution of the above starting material (3a) in dichloromethane (13 parts) under nitrogen are added at -5° to 0° C. pyridine (2 equivalents) and at -30° to -25° C. phosphorus pentachloride (1.7 equivalents). The mixture is stirred at -15° to -10° C. for 4 hours, cooled to -25° to -30° C., mixed with isobutanol (10 parts) cooled at -30° to -20° C., and let stand at 0° to 5° C. overnight. The reaction mixture is cooled to -20° to -25° C., mixed dropwise with triethylamine (10.9 equivalents), and kept at 0° to 5° C. overnight. The reaction mixture is diluted with dichloromethane (20 parts) and ice water (20 parts) and stirred for 20 minutes. The formed organic layer is taken, washed with hydrochloric acid, water, aqueous sodium hydrogen carbonate, and water, dried, and concentrated. The residue is crystallized from ethyl acetate to give 7beta-amino-3-cephem-4-carboxylic acid diphenylmethyl ester (5). Yield: 60.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04647658
Source datasetuspto-grants-1987_03
ORD IDord-2d708f4cb9db412e9e4c4a63bc6cbfdf
Source noteuspto-grants-1987_03