HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341640Generated: October 30, 2026
Potassium Phosphate, Tribasic → Dasabuvir
https://huagongshe.com/reaction/341640
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | 1-Butanesulfonic acid, 1,1,2,2,3,3,4,4,4-nonafluoro-, 6-(5-(3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinyl)-3-(1,1-dimethylethyl)-2-methoxyphenyl)-2-naphthalenyl ester | HCID 56640669 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Catalyst | Di-tert-butyl(2',4',6'-triisopropyl-3,6-dimethoxy-(1,1'-biphenyl)-2-yl)phosphine | HCID 44233348 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Dasabuvir | HCID 56640146 | 236.8% |
Reaction Steps
A 450-mL, stainless steel Parr pressure reactor equipped with an overhead stirrer was charged with tris(dibenzylideneacetone)dipalladium(0) (0.131 g, 0.143 mmol), di-tert-butyl(2′,4′,6′-triisopropyl-3,6-dimethoxybiphenyl-2-yl)phosphine (0.167 g, 0.344 mmol) and milled potassium phosphate tribasic (6.69 g, 31.5 mmol). The flask was purged with argon for not less than 90 minutes. Ethyl acetate (80 mL) was taken in a 100-mL, round bottom flask, purged with argon for not less than 30 minutes and was transferred to the 450-mL reactor using a cannula under argon atmosphere. The contents of the 450-mL reactor were heated to 80° C. and stirred at this temperature for 30 minutes. A 250-mL round bottom flask equipped with a magnetic stir bar was charged with 6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate (20.0 g, 22.9 mmol), methanesulfonamide (3.27 g, 34.4 mmol) and ethyl acetate (160 mL), purged with argon for not less than 60 minutes while stirring at 50° C. This solution was transferred to the 450-mL reactor that has been cooled to the room temperature using a cannula under argon atmosphere. The temperature of the 450-mL flask was raised to 90° C. and the contents were stirred for 15 hours. The reaction mixture was allowed to cool down to the room temperature, filtered and rinsed with ethyl acetate (120 mL). Solid (26.76 g) was obtained after drying the solid for 2 hours on high vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08895737B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-61792153fb6a45cba642653639200174 |
|---|
| Source note | uspto-grants-2014_11 |
|---|