HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776841Generated: November 1, 2026
Potassium Phosphate, Tribasic → HCID 86728247, compound
https://huagongshe.com/reaction/1776841
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | 2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuran-3-carboxamide | HCID 68239402 | — |
| Reactant | HCID 86728248 | HCID 86728248 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86728247 | HCID 86728247 | 84% |
Reaction Steps
To a degassed solution of methyl 2-chloro-6H-pyrido[2′,3′:5,6][1,3]oxazino[3,4-a]indole-11-carboxylate (40 mg, 0.13 mmol) and 2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuran-3-carboxamide (50 mg, 0.10 mmol) in 1,4-dioxane (3 mL), Pd2(dba)3 (10 mg), X-Phos (10 mg) and K3PO4 (60 mg, 0.23 mmol) were added under N2. The mixture was heated to 100° C. for 2 hours. The reaction mixture was cooled to RT, filtered and washed with EtOAc. The filtrate was washed with H2O, brine, dried over Na2SO4. After concentrated, the resulting residue was purified using column chromatography (dichloromethane:MeOH=100:1) to provide the product of methyl 2-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)-6H-pyrido[2′,3′:5,6][1,3]oxazino[3,4-a]indole-11-carboxylate (55 mg, yield: 84%). MS (M+H)+: 655.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09265773B2 |
|---|
| Source dataset | uspto-grants-2016_02 |
|---|
| ORD ID | ord-51f20e9d0b58426e9a16ca697ba64b2e |
|---|
| Source note | uspto-grants-2016_02 |
|---|