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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033287Generated: November 2, 2026

Methanesulfonyl chloride → HCID 22851615, compound

https://huagongshe.com/reaction/1033287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 12081666HCID 12081666—
SolventPyridineHCID 1049—
ProductHCID 22851615HCID 2285161590%

Reaction Steps

After 1 g (2.7 mmols) of 5'-O-acetyl-3'-deoxy-3'-bromoadenosine was added to 10 ml of pyridine, 340 mg (1.1 eq.) of methanesulfonyl chloride was added to the mixture. The mixture was stirred at room temperature for 30 minutes and pyridine was distilled off under reduced pressure. The residue was added to 30 ml of water followed by extraction twice with 30 ml of chloroform. After the organic solvent was washed with water and then dried over magnesium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography to give 1.09 g (yield, 90%) of 2'-O-mesyl-5'-O-acetyl-3'-deoxy-3'-bromoadenosine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310895
Source datasetuspto-grants-1994_05
ORD IDord-043f0fb5557e47c6b01699a6d97a5264
Source noteuspto-grants-1994_05