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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797206Generated: October 31, 2026

Methanesulfonyl chloride → HCID 22176582, compound

https://huagongshe.com/reaction/1797206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 22176548HCID 22176548—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22176582HCID 22176582—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 250 mL 3 neck flask fitted with a stirrer and thermometer, 285 mg of methanesulfonyl chloride is added dropwise to 350 mg of {2-[4-(3-aminophenyl)phenyl]-2-fluoropropyl}[(dimethylamino)sulfonyl]amine (prepared in example 38) and 380 mg of DBU in THF (125 mL) while stirring at 0° C. under a nitrogen atmosphere. The reaction is allowed to warm to room temperature and then stirred overnight at this temperature. In the morning, the reaction is concentrated under reduced vacuum. The resulting material is taken into ethyl acetate and the organic layer is washed two times with H2O, dried over Na2SO4, filtered, and concentrated under reduced vacuum. This crude material is purified via silica gel chromatography employing the Chromatotron and using a 4000 micron rotor with hexane/ethyl acetate eluent to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034045B1
Source datasetuspto-grants-2006_04
ORD IDord-967dfe1aa32b4af9b75599825c9725f6
Source noteuspto-grants-2006_04