Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295619Generated: November 1, 2026

N,N-Dimethylaniline → 4-Nitrobenzyl 7-amino-3-hydroxy-3-cephem-4-carboxylate

https://huagongshe.com/reaction/2295619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant(6S)-4-Nitrobenzyl 3-hydroxy-8-oxo-7-(N-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylateHCID 67685788—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product4-Nitrobenzyl 7-amino-3-hydroxy-3-cephem-4-carboxylateHCID 6812323569.5%

Reaction Steps

Triethylamine (2.37 g.), dimethylaniline (7.12 g.) and trimethylsilyl chloride (3.93 g.) were added to a stirred suspension of 4-nitrobenzyl 7-(2-phenylacetamido)-3-hydroxy-3-cephem-4-carboxylate (10 g.) in methylene chloride (200 ml.) in turn, and the solution was stirred at room temperature for an hour. Phosphorus pentachloride (4.88 g.) was added to the solution at -30° to -25° C. and stirred at -25° to -20° C. for 3 hours. Methanol (42 ml.) was added to the solution at -25° to -20° C., and stirred for an hour. To the solution was added water (35 ml.) at -25° to -20° C., and the solution was stirred at room temperature. The precipitates were collected by filtration, washed with methylene chloride and diethyl ether in turn, and dried to give 4-nitrobenzyl 7-amino-3-hydroxy-3-cephem-4-carboxylate (5.2 g.), mp 148° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04425341
Source datasetuspto-grants-1984_01
ORD IDord-be99a8ff37ab403bb0c4bf06fe2bc8eb
Source noteuspto-grants-1984_01