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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200210Generated: October 27, 2026

Pyridine → 3',5'-DI-O-Mesylthymidine

https://huagongshe.com/reaction/1200210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThymidineHCID 5789—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventWaterHCID 962—
Product3',5'-DI-O-MesylthymidineHCID 1057293281.2%

Reaction Steps

A 3 liter, 3 necked round-bottomed flask was equipped with an overhead stirrer and paddle, a 500 mL dropping funnel and a Claisen adapter containing a drying tube and a thermometer. Thymidine (200 g, 0.82M) and pyridine (750 mL) were added to the flask. The mixture was stirred and warmed with a water bath (20 mins) to give a clear solution. The solution was then cooled in an ice bath to 0°-3° C. and the dropping funnel was charged with methanesulfonyl chloride (206.5 g, 1.08M). The methanesulfonyl chloride was then added dropwise over 40 minutes with no noticeable exotherm. The solution was stirred at 0° C. for 1 hr and then stored at 5° C. for 18 hr. The light brown mixture was then poured onto rapidly stirred water (3 L) containing ice (approx. 500 g). The desired product crystallised immediately. After stirring for 0.5 hr, the product was collected by filtration and washed several times with water (3×100 mL). The white solid was then dried under vacuum overnight (crude weight, 322 g, 98% yield). The product was recrystallised from hot acetone to give 267 g of a white solid (81% yield), mp 169°-171° C. (lit. 170°-171° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04904770
Source datasetuspto-grants-1990_02
ORD IDord-17da8516b1664f038c03b80c8c77207a
Source noteuspto-grants-1990_02