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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885852Generated: October 31, 2026

Methanesulfonyl chloride → HCID 59312564, compound

https://huagongshe.com/reaction/885852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86641369HCID 86641369—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59312564HCID 5931256446.1%

Reaction Steps

Methanesulfonyl chloride (0.41 ml, 5.3 mmol) was added to a stirred solution of (E)-3-{4-[(E)-3-(3-hydroxymethyl-phenyl)-3-oxo-propenyl]-phenyl}-N-(tetrahydro-pyran-2-yloxy)-acrylamide (1.08 g, 2.68 mmol) and TEA (1.47 ml, 10.6 mmol) in DCM (18 ml) and DMF (12 ml). The mixture was stirred at room temperature for 30 min and then brought to basic conditions with 5% NaHCO3. The resulting slurry was extracted with Et2O and the organic phase was washed with water, dried over Na2SO4 and evaporated in vacuo. The crude reaction mixture was purified by column chromatography (eluent: petroleum ether/AcOEt 1:1) to give 600 mg of a mixture of the title compound and (E)-3-{4-[(E)-3-(3-chloromethyl-phenyl)-3-oxo-propenyl]-phenyl}-N-(tetrahydro-pyran-2-yloxy)-acrylamide as the main product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242175B2
Source datasetuspto-grants-2012_08
ORD IDord-325ca64576114d0db10606d295dfa6ac
Source noteuspto-grants-2012_08