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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683176Generated: October 27, 2026

Pyridine → HCID 88370434, compound

https://huagongshe.com/reaction/1683176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactantbenzhydryl (E)-(2S,3S,5R)-3-(3-hydroxy-propenyl)-3-methyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylateHCID 10645194—
SolventDichloromethaneHCID 6344—
ProductHCID 88370434HCID 88370434—

Reaction Conditions

Temperature-40 °C

Reaction Steps

410 mg (1.0 mmol) of benzhydryl (E)-(2S,3S,5R)-3-(3-hydroxy-propenyl)-3-methyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2carboxylate were dissolved in 6 ml of methylene chloride, cooled to -40° C. and treated with 250 μl (1.5 mmol) of trifluoromethanesulfonic anhydride. After 5 minutes 200 μl (2.50 mmol) of pyridine were added, the mixture was stirred at the same temperature for a further hour and subsequently the cooling bath was removed. The solvent was removed on a rotary evaporator at room temperature, the reaction mixture was taken up in 20 ml of methylene chloride and washed twice with 10 ml of saturated sodium chloride solution each time. Drying over magnesium sulfate, filtration and concentration on a rotary evaporator were carried out. The residual red resin was oxidized without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637579
Source datasetuspto-grants-1997_06
ORD IDord-6251722413164964b4cf6b00b2927f0f
Source noteuspto-grants-1997_06