Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522230Generated: October 29, 2026

Cesium carbonate → tert-butyl 4-(4-(2-(methylamino)pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridin-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate

https://huagongshe.com/reaction/522230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantTricyclohexylphosphineHCID 75806—
ReactantN-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)pyridin-2-amineHCID 72218845—
Reactanttert-butyl 4-(4-bromo-1H-pyrrolo[2,3-b]pyridin-2-yl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 118274390—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
Producttert-butyl 4-(4-(2-(methylamino)pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridin-2-yl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 118274083—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of Example 135D (170 mg, 0.45 mmol), N-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine (105 mg, 0.45 mmol), bis(triphenylphosphine)palladium(II) chloride (31 mg, 0.045 mmol), tricyclohexylphosphine (13 mg, 0.045 mmol) and cesium carbonate (443 mg, 1.34 mmol) in a round bottom flask was purged with nitrogen. Dioxane (10 mL) was added and the mixture was heated at 100° C. overnight. After cooling, the mixture was triturated with dichloromethane (200 mL) and filtered. The filtrate was concentrated and the residue was separated by flash chromatography on silica gel (Teledyne CombiFlash Rf, 40% to 100% ethyl acetate in hexane) to provide the title compound. MS (ESI+) m/z 406 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328112B2
Source datasetuspto-grants-2016_05
ORD IDord-ffaee0bba07147e3aa9536e63fd3dd65
Source noteuspto-grants-2016_05