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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359340Generated: October 30, 2026

Acetic Acid → 2-Benzyl-3-iodo-6-[(3S,4S)-3-acetoxy-4-methoxypyrrolidine-1-yl)pyridine

https://huagongshe.com/reaction/1359340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCesium carbonateHCID 10796—
Reactant2-benzyl-3-iodo-6-[(3S,4S)-3-(3-nitrobenzenesulfonyl)oxy-4-methoxypyrrolidin-1-yl]pyridineHCID 21058021—
SolventDimethyl SulfoxideHCID 679—
Product2-Benzyl-3-iodo-6-[(3S,4S)-3-acetoxy-4-methoxypyrrolidine-1-yl)pyridineHCID 131723996—

Reaction Steps

4.2 ml of acetic acid was added to a mixture of 7.9 g of cesium carbonate and 15 ml of dimethyl sulfoxide. After foaming stopped, a mixture of 14.4 g of 2-benzyl-3-iodo-6-[(3S,4S)-3-(3-nitrobenzenesulfonyl)oxy-4-methoxypyrrolidine-1-yl]pyridine and 35 ml of dimethyl sulfoxide was added thereto, followed by heating under stirring for 6 hours in an oil bath kept at 70° C. in a nitrogen atmosphere. The reaction solution was cooled and then subjected to extraction with ethyl acetate-water. The organic phase was washed with water and brine brine, dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography using 10-15% ethyl acetate/hexane, to give 7.5 g of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599917B1
Source datasetuspto-grants-2003_07
ORD IDord-1e6587ff034f47f3b2b7f34f4a7b2dcf
Source noteuspto-grants-2003_07