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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40878Generated: October 26, 2026

Tetraethylammonium → (2e)-3-[3-Methyl-1-(1h-pyrrolo[2,3-b]pyridin-4-yl)-1h-pyrazol-4-yl]acrylonitrile

https://huagongshe.com/reaction/40878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetraethylammoniumHCID 5413—
ReactantDimethylformamideHCID 6228—
ReactantAcrylonitrileHCID 7855—
Reactant4-(4-bromo-3-methyl-1H-pyrazol-1-yl)-1H-pyrrolo[2,3-b]pyridineHCID 17754465—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
Product(2e)-3-[3-Methyl-1-(1h-pyrrolo[2,3-b]pyridin-4-yl)-1h-pyrazol-4-yl]acrylonitrileHCID 17754407191.3%

Reaction Steps

A solution of 2-propenenitrile (0.043 mL, 0.00065 mol), bis(triphenylphosphine)palladium(II) chloride (0.0091 g, 0.000013 mol), 4-(4-bromo-3-methyl-1H-pyrazol-1-yl)-1H-pyrrolo[2,3-b]pyridine (0.036 g, 0.00013 mol), and tetraethylamine (TEA) (0.15 mL, 0.0011 mol) in DMF (0.15 mL, 0.0019 mol) was microwaved at 120° C. for 2 h. The solution was then diluted with ethyl acetate and washed with water (×2) and brine successively. The organic phase was dried and concentrated in vacuo to give 62 mg of the product as an orange solid. The orange solid was purified by prep-LCMS to give 12 mg of an off-white solid as a trifluoroacetic acid (TFA) salt which was triturated with MTBE (1 mL) to provide the purified product as a pale green solid. (dried at 60° C. for 4 h, 9 mg , 28% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530485B2
Source datasetuspto-grants-2013_09
ORD IDord-06f7be7fd5214d2597c15024016d6fb9
Source noteuspto-grants-2013_09