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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351152Generated: November 2, 2026

Pyridine → HCID 131716167, compound

https://huagongshe.com/reaction/2351152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiisopropyl EtherHCID 7914—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantHCID 131716168HCID 131716168—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 131716167HCID 131716167—

Reaction Steps

To a suspension of phosphorus pentachloride (366 mg) in methylene chloride (6ml) was added pyridine (0.142 ml) at -30° C. After the mixture was stirred for 30 minutes at the same temperature, p-nitrobenzyl 7-(2-phenylacetamido)-3-vinylthio-3-cephem-4-carboxylate (300 mg) was added thereto at -30° C. The mixture was stirred for 1 hour under the ice-cooling to the mixture was added methanol (0.38 ml) at -30° C., and the mixture was stirred for 2 hours at -15 ~-20° C. Water (0.4 ml) was added thereto under ice-cooling. Diisopropyl ether (5 ml) was added to the mixture to give a precipitate. The precipitate was collected, washed with water and diisopropyl ether successively and dried over phosphorus pentoxide to give p-nitrobenzyl 7-amino-3-vinylthio-3-cephem-4-carboxylate hdrochloride (181 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871730
Source datasetuspto-grants-1989_10
ORD IDord-e19839d8541f4f7285f7907b4cdf1336
Source noteuspto-grants-1989_10