Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 59442022 | HCID 59442022 | — |
| Reactant | HCID 86644195 | HCID 86644195 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 67315992 | HCID 67315992 | 96% |
Reaction Steps
To a suspension of 6-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-2,3-difluorobenzamide (600 mg, 1.26 mmol) in 2,2,2-trifluoroethanol (40 ml) was added 1-[(dimethylamino)acetyl]-6-(methyloxy)-1,2,3,4-tetrahydro-7-quinolinamine (366 mg, 1.39 mmol), hydrochloric acid as a 4.0M solution in dioxane (2.51 ml, 10.1 mmol), and catalytic potassium iodide (<10 mg). The resulting slurry was stirred at 90° C. in a pressure vial for 24 hours, at which time all solids had completely dissolved. The resulting solution was cooled to room temperature and diluted with dichloromethane and saturated sodium bicarbonate as to adjust the aqueous layer to pH>10. The organic layer was washed with water and a saturated brine solution, dried over sodium sulfate, filtered and solvents were removed under reduced pressure. The resulting green solid was purified via trituration with diethyl ether to afford 5-{[1-(N,N-dimethylglycyl)-6-(methyloxy)-1,2,3,4-tetrahydro-7-quinolinyl]amino}-8,9-difluoro-3-[(4-methylphenyl)sulfonyl]pyrrolo[2′,3′:4,5]pyrimido[6,1-b]quinazolin-7(3H)-one (830 mg, 1.21 mmol) as a yellow solid. (ESIMS (M+H)+=688)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981903B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-35a6a8586eba4ca4aab5c9b7d3e3387b |
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| Source note | uspto-grants-2011_07 |
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