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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081924Generated: October 25, 2026

Pristinamycin → Virginiamycin M1

https://huagongshe.com/reaction/1081924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPristinamycinHCID 11979535—
SolventDichloromethaneHCID 6344—
ProductVirginiamycin M1HCID 54593190.6%

Reaction Steps

A simplified modification of the procedure of Sharma, et el. is suitable for use in the invention. In this procedure, 500 g STAFAC® is placed in an Erlenmeyer flask with 3.75 L methylene chloride. The mixture is stirred overnight with a mechanical stirrer. The STAFAC® is filtered, and rinsed with a Buchner funnel under vacuum, giving a cloudy yellow solution. A second filtration is performed through a glass-frit (medium) filter, giving a clear yellow solution. This solution is concentrated in vacuo to give a crude mixture of VM and VS. 10 g of this yellow/brown solid is purified with a medium pressure liquid chromatography (MPLC) column using gradients of 0.5, 1, 1.5, 3, 4, 6 and 8% methyl alcohol in methylene chloride. The fractions are separated by thin layer chromatography, and the fraction containing VM is concentrated with rotary evaporation. The VM1 is then recrystallized using ethyl acetate. 1.105 g of virginiamycin M1 is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587475
Source datasetuspto-grants-1996_12
ORD IDord-2953ea09ad214178a1f415aabe2c45e3
Source noteuspto-grants-1996_12