HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590853Generated: October 30, 2026
Cesium carbonate → 1-(3-(methylamino)-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(phenyl(tetrahydrofuran-2-yl)methyl)urea
https://huagongshe.com/reaction/590853
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-(Phenyl(tetrahydrofuran-2-yl)methyl)urea | HCID 118271757 | — |
| Reactant | 6-chloro-N-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine | HCID 118272406 | — |
| Catalyst | BrettPhos Palladacycle | HCID 25112666 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(3-(methylamino)-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(phenyl(tetrahydrofuran-2-yl)methyl)urea | HCID 118272251 | — |
Reaction Steps
6-chloro-N-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine (400 mg, 0.941 mmol), 1-(phenyl(tetrahydrofuran-2-yl)methyl)urea (228 mg, 1.035 mmol), cesium carbonate (920 mg, 2.82 mmol) and BrettPhos precatalyst (52.6 mg, 0.066 mmol) were taken up in dioxane (9.5 ml) in a 20 mL microwave vial. The vial was evacuated and back-filled with N2 (×3). The reaction mixture was stirred at 100° C. for two hours. Room temperature was attained. The crude reaction mixture was diluted with EtOAc and filtered through celite. The filtrate was concentrated in vacuo, taken up in 5 ml of DCM, and purified on silica gel 5-50% DCM/EtOAc to give 1-(3-(methylamino)-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(phenyl(tetrahydrofuran-2-yl)methyl)urea. MS ESI calc'd. for C38H37N6O2 [M+H]+ 609. found 609.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09233979B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-b7386dca42fa491a9c416b6f4f663130 |
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| Source note | uspto-grants-2016_01 |
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