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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252015Generated: October 25, 2026

Chloroform → {3-[1-(3,5-bis-trifluoromethyl-benzyl)-5-pyridin-4-yl-1H-[1,2,3]triazol-4-yl]-pyridin-2-yl}-(2-chloro-phenyl)-methanone

https://huagongshe.com/reaction/2252015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantTrifluoro-methanesulfonic acid 2-(2-chloro-benzoyl)-pyridin-3-yl esterHCID 85882776—
Reactant4-[3-(3,5-bis(trifluoromethyl)benzyl)-5-tributylstannanyl-3H-[1,2,3]triazol-4-yl]-pyridineHCID 86601244—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product{3-[1-(3,5-bis-trifluoromethyl-benzyl)-5-pyridin-4-yl-1H-[1,2,3]triazol-4-yl]-pyridin-2-yl}-(2-chloro-phenyl)-methanoneHCID 1028993011%

Reaction Conditions

Temperature120 °C

Reaction Steps

Add Pd2(dba)3.CHCl3 (42 mg, 0.04 mmol) to a degassed solution of trifluoro-methanesulfonic acid 2-(2-chloro-benzoyl)-pyridin-3-yl ester (149 mg, 0.41 mmol) and 4-[3-(3,5-bis-trifluoromethyl-benzyl)-5-tributylstannanyl-3H-[1,2,3]triazol-4-yl]-pyridine (296 mg, 0.45 mmol) in toluene (2 mL). Seal the mixture under N2 and heat at 120° C. for 2 hours. Add Pd(PPh3)4 (94 mg, 0.08 mmol), seal and heat at 120° C. for another 48 hours. Concentrate, dissolve in ACN, wash with hexanes (×3), dry over MgSO4 and concentrate. Purify the residue by flash chromatography on silica gel eluting with 0-10% ACN/Et2O to afford the title compound (26 mg, 11%) as tan solid. MS(IS) 588 (M+1). TLC: Rf=0.33 (10% ACN/Et2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320994B2
Source datasetuspto-grants-2008_01
ORD IDord-8e6565be9ed94175863b7814513ac7bf
Source noteuspto-grants-2008_01