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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629052Generated: October 26, 2026

Water → 3-(5-Cyanopyridin-3-yl)-N-(4-(trifluoromethoxy)phenyl)benzamide

https://huagongshe.com/reaction/629052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant3-bromo-N-(4-(trifluoromethoxy)phenyl)benzamideHCID 1371033—
Reactant5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinonitrileHCID 16414216—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-(5-Cyanopyridin-3-yl)-N-(4-(trifluoromethoxy)phenyl)benzamideHCID 72202877—

Reaction Steps

3-bromo-N-(4-(trifluoromethoxy)phenyl)benzamide (Stage 3.1, 50 mg, 0.139 mmol), 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinonitrile (0.180 mmol), 2 M Na2CO3 (0.104 mL, 0.208 mmol), (Ph3P)4Pd (8 mg, 6.94 μmol), water (0.8 mL) and DME (2.4 mL) were added to a vial, which was sealed and subjected to MW irradiation at 150° C. for 10 min. The RM was filtered through a PL-Thiol MP SPE cartridge (StratoSpheres™, 6 mL) and the cartridge was washed with MeOH (10 mL). The combined filtrates were evaporated to dryness under reduced pressure and the crude product was purified by preparative HPLC to afford the title compound. LC-MS (Condition 5) tR=1.24 min, m/z=384.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315489B2
Source datasetuspto-grants-2016_04
ORD IDord-5a68f57126e143c78592be4913799d4b
Source noteuspto-grants-2016_04