HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048034Generated: October 31, 2026
Methanesulfonamide → HCID 58042509, compound
https://huagongshe.com/reaction/2048034
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 86660844 | HCID 86660844 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58042509 | HCID 58042509 | 64.9% |
Reaction Steps
Methanesulphonamide (89.54 mg, 0.94 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.15 mL, 1.03 mmol) were added to 4-methylphenyl-5-chloro-4-(6-(2,2,3,3-tetrafluoropropoxy)-5-(trifluoromethyl)pyridin-3-yloxy)-2-fluorobenzoate (Preparation 263, 475 mg, 0.86 mmol) in acetonitrile (5 mL) and the reaction mixture was stirred for 18 hours at room temperature. The reaction was concentrated in vacuo and the residue was partitioned between ethyl acetate and water, the organic layer was separated, dried over anhydrous magnesium sulfate, filtered and the filtrate was concentrated in vacuo. The crude product was purified by reverse phase chromatography (acetonitrile/water both with 0.1% formic acid) to give the title compound as a white solid (303 mg, 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08592629B2 |
|---|
| Source dataset | uspto-grants-2013_11 |
|---|
| ORD ID | ord-26d05ad8164a4697b883aa39b80b8693 |
|---|
| Source note | uspto-grants-2013_11 |
|---|