Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157786Generated: October 25, 2026

Potassium Carbonate → N-(1-(4-methoxy-1H-pyrrolo[2,3-c]pyridin-7-yl)-1H-1,2,4-triazol-3-yl)pivalamide

https://huagongshe.com/reaction/1157786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
Reactant7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridineHCID 20791244—
ReactantN-(1H-1,2,4-triazol-3-yl)pivalamideHCID 178447248—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductN-(1-(4-methoxy-1H-pyrrolo[2,3-c]pyridin-7-yl)-1H-1,2,4-triazol-3-yl)pivalamideHCID 5951146026%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine (250 mg, 1.101 mmol), potassium carbonate (457 mg, 3.30 mmol), copper(I) iodide (105 mg, 0.551 mmol), N-(1H-1,2,4-triazol-3-yl)pivalamide and (1R,2R)—N1,N2-dimethylcyclohexane-1,2-diamine (78 mg, 0.551 mmol) in 1,4-dioxane (2 mL) were heated up at 110° C. for 13 h. The reaction mixture was filtered through a silica gel pad and concentrated under reduced pressure. The resulting crude was purified by prep HPLC to give N-(1-(4-methoxy-1H-pyrrolo[2,3-c]pyridin-7-yl)-1H-1,2,4-triazol-3-yl)pivalamide (90 mg, 26%) as pale yellow oil. LCMS: m/e 315.05 (M+H)+, ret time 1.55 min (method 8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807676B2
Source datasetuspto-grants-2010_10
ORD IDord-80c371fb3593471aadecb0494cfb88c7
Source noteuspto-grants-2010_10