HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590794Generated: October 30, 2026
Cesium carbonate → (R)-1-(1-(4-fluorophenyl)ethyl)-3-(3-(methylamino)-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)urea
https://huagongshe.com/reaction/590794
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | (R)-1-(1-(4-fluorophenyl)ethyl)urea | HCID 117601722 | — |
| Reactant | 6-chloro-N-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine | HCID 118272406 | — |
| Catalyst | Brettphos | HCID 25112535 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (R)-1-(1-(4-fluorophenyl)ethyl)-3-(3-(methylamino)-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)urea | HCID 118272252 | — |
Reaction Steps
6-Chloro-N-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine (332 mg, 0.781 mmol), (R)-1-(1-(4-fluorophenyl)ethyl)urea (Intermediate 20C; 193 mg, 1.059 mmol), BrettPhos pre-catalyst (48.0 mg, 0.060 mmol), and cesium carbonate (759 mg, 2.330 mmol) were taken up in 1,4-dioxane (6 mL) in a 20 mL microwave vial. The vial was evacuated and back-filled with N2 (×3) and the reaction was stirred at 100° C. for 3 h. Room temperature was attained, the reaction mixture was filtered through Celite, eluting with MeOH, and the filtrate was concentrated in vacuo. Purification of the residue by flash chromatography (0-100% EtOAc-DCM) gave (R)-1-(1-(4-fluorophenyl)ethyl)-3-(3-(methylamino)-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)urea. MS ESI calc'd. For C35H31FN6O [M+1]+ 571. found 571.
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-31a54a8e85754d888bcdca60f0dcc2db |
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| Source note | uspto-grants-2016_01 |
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