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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292843Generated: October 30, 2026

Methanesulfonyl chloride → HCID 58904611, compound

https://huagongshe.com/reaction/1292843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 58904652HCID 58904652—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58904611HCID 5890461166%

Reaction Steps

To a mixture of 77 mg (0.2 mmol) of 2-[4-(3-aminophenyl)piperazino]ethyl-N-(2-ethoxyphenyl)carbamate derivative and 56 μl (0.4 mmol, 2 eq) of TEA in 5 ml of THF, 31 μl (0.4 mmol, 2 eq) of mesyl chloride is added. Shaking is carried out at room temperature for about 20 hours. After concentration under reduced pressure, H2O is added and the aqueous phase is extracted with CH2Cl2. After drying on Na2SO4 and concentration of the organic phase, a brown oil is obtained which is purified by column chromatography (eluent AcOEt/petroleum ether 8:2) to produce 61 mg of the expected product as a brown oil (yield: 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238693B2
Source datasetuspto-grants-2007_07
ORD IDord-3d67b5bb449742b09aeca48f50dd2d3f
Source noteuspto-grants-2007_07