HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987224Generated: October 26, 2026
Dimethyl Sulfoxide → HCID 11516373, compound
https://huagongshe.com/reaction/1987224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | N-(4-fluoro-3-nitrophenyl)ethanesulfonamide | HCID 3286362 | — |
| Reactant | 1-(4,4-Difluorocyclohexyl)methanamine | HCID 15604494 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11516373 | HCID 11516373 | 63.8% |
Reaction Steps
N-(4-Fluoro-3-nitrophenyl)ethanesulfonamide (26 g, 0.107 mol), [(4,4-difluorocyclohexyl)methyl]amine (approx. 15 g), DIPFA (20 mL) and DMSO (100 mL) were mixed together and heated to 65° C. overnight. Ethanolamine (5 g) was added and the reaction mixture was stirred until complete disappearance of N-(4-fluoro-3-nitrophenyl)ethanesulfonamide (approx. 4-5 hrs.). The room temperature cooled down reaction mixture was poured in cold water (900 mL). The product was extracted with DCM (5×200 mL). The combined organic phases were washed with HCl 2N (3×200 mL) and dried over anhydrous Na2SO4. The solvent was removed and the crude product was purified on silica gel by flash chromatography (this material can be re-crystallized using a mixture of EtOAc and hexane) to provide the title product (24.2 g) as orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07550495B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-98c8825b80c04d309453a53714842663 |
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| Source note | uspto-grants-2009_06 |
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