HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359272Generated: October 31, 2026
Methanesulfonamide → HCID 56592716, compound
https://huagongshe.com/reaction/2359272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 13105473 | HCID 13105473 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 56592716 | HCID 56592716 | 170.2% |
Reaction Steps
To a solution of 4-(3-(trifluoromethyl)phenylamino)benzoic acid (150 mg, 0.533 mmol) in DMF (4 mL) were added HATU (243 mg, 0.640 mmol), methanesulfonamide (152 mg, 1.60 mmol) and DIPEA (0.296 mL) and the reaction stirred at room temperature for 16 hours. Methanesulfonamide (152 mg, 1.60 mmol) was added and the reaction stirred at room temperature for 72 hours. After this time the reaction was quenched by the addition of potassium hydrogen sulfate (20 mL) and the aqueous extracted with dichlormethane (3×20 mL). The combined organics were washed with brine (40 mL), filtered through a phase separation cartridge and then the solvent was removed under reduced pressure to give an oil (325 mg). The crude was purified by preparative HPLC to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08685977B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-a856cadb52654557a39311d68f35bc06 |
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| Source note | uspto-grants-2014_04 |
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