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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798378Generated: November 1, 2026

Sodium Carbonate → 6-(3-Methyl-1-trityl-1H-pyrazol-4-yl)-nicotinonitrile

https://huagongshe.com/reaction/1798378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant6-Chloro-3-pyridinecarbonitrileHCID 5152094—
Reactant(3-Methyl-1-trityl-1H-pyrazol-4-yl)boronic acidHCID 22031628—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product6-(3-Methyl-1-trityl-1H-pyrazol-4-yl)-nicotinonitrileHCID 5933197153%

Reaction Conditions

Temperature135 °C

Reaction Steps

To a solution of 6-Chloro-nicotinonitrile (0.2 g, 1.49 mmol) and 3-methyl-1-trityl-1H-pyrazole-4-boronic acid* (0.5 g, 1.36 mmol) in ethylene glycol dimethyl ether (3 ml), was added sodium carbonate (0.36 g, 3.39 mmol) in water (1.5 ml). The reaction mixture was degassed with nitrogen before addition of tetrakis(triphenylphosphine)palladium (0) and then heated in a CEM microwave at 135° C. for 30 minutes (50 W power). Reaction partitioned between water and ethyl acetate, aqueous basified with 2N NaOH, organic extracts were combined, dried (MgSO4) and solvent removed. Crude product suspended in small volume of methanol, white precipitate filtered to afford the title compound (0.32 g, 53% yield). LC/MS: (PS-A2) Rt 4.52 [M+H]+427.26. *This starting material can be made by the method described in EP1382603A1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343953B2
Source datasetuspto-grants-2013_01
ORD IDord-2d639a93871d4cf684454838b5440a50
Source noteuspto-grants-2013_01