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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177563Generated: October 30, 2026

2-Chloro-3-(trifluoromethyl)benzoyl chloride → HCID 90409113, compound

https://huagongshe.com/reaction/2177563

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-3-(trifluoromethyl)benzoyl chlorideHCID 3827633—
Reactant1-(5-Fluoropyridin-2-yl)-1H-imidazo[4,5-c]pyridineHCID 90409583—
ReactantHCID 178418689HCID 178418689—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90409113HCID 9040911354%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of Intermediate 1 (0.70 g, 3.27 mmol) in THF (20 mL) was added Intermediate 12 (0.87 g, 3.60 mmol) dropwise. The reaction was allowed to stir for 1 h then cooled to −78° C. To the cooled solution was added 3M MeMgBr in Et2O (1.31 mL, 3.92 mmoL) and the reaction was let come to room temperature. The mixture was then quenched with 1N NaOH (50 mL) and extracted with EtOAc (3×30 mL). The organic layers were combined, dried (Na2SO4), and concentrated. Chromatography of the resulting residue (SiO2; MeOH (NH3):DCM) gave the title compound (770 mg, 54%). 1H NMR (400 MHz, CDCl3) δ 8.43-8.34 (m, 1H), 7.92-7.73 (m, 2H), 7.70-7.33 (m, 4H), 6.08 (dtd, J=19.7, 11.7, 8.0 Hz, 3H), 1.54 (t, J=7.0 Hz, 3H). MS (ESI): mass calculated for C20H13ClF4N4O, 436.07. m/z found 437.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09066946B2
Source datasetuspto-grants-2015_06
ORD IDord-f90cd87a42234a698026c8852db31c31
Source noteuspto-grants-2015_06