HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797206Generated: October 31, 2026
Methanesulfonyl chloride → HCID 22176582, compound
https://huagongshe.com/reaction/1797206
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 22176548 | HCID 22176548 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22176582 | HCID 22176582 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07034045B1 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-967dfe1aa32b4af9b75599825c9725f6 |
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| Source note | uspto-grants-2006_04 |
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