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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282293Generated: November 1, 2026

Phenylsilane → N-{4-[4-(2,4-Dichlorophenyl)-5-(1H-imidazol-2-yl)-1,3-thiazol-2-yl]pyridin-2-yl}acetamide

https://huagongshe.com/reaction/2282293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylsilaneHCID 12752—
ReactantN-{4-[5-(1-Allyl-1H-imidazol-2-yl)-4-(2,4-dichlorophenyl)-1,3-thiazol-2-yl]pyridin-2-yl}acetamideHCID 58094968—
CatalystHCID 178418397HCID 178418397—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductN-{4-[4-(2,4-Dichlorophenyl)-5-(1H-imidazol-2-yl)-1,3-thiazol-2-yl]pyridin-2-yl}acetamideHCID 5809526264%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of N-{4-[5-(1-Allyl-1H-imidazol-2-yl)-4-(2,4-dichlorophenyl)-1,3-thiazol-2-yl]pyridin-2-yl}acetamide (0.0650 g, 0.138 mmol) in dichloromethane (1.0 mL) and acetic acid (0.34 mL) was added tetrakis(triphenylphosphine)palladium(0) (0.00798 g, 0.00691 mmol) followed by phenylsilane (0.0870 mL, 0.706 mmol). The solution was stirred at 40° C. for 90 minutes. The solution was cooled to room temperature then concentrated in vacuo and diluted with ethyl acetate and saturated sodium bicarbonate solution. The layers were separated and the aqueous phase was extracted 3 more times with ethyl acetate. The organic extracts were washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. Column chromatography was performed to yield the title compound (0.0380 g, 64%). LCMS: (FA) ES+, 431, 433. 1H NMR (400 MHz, d4-Methanol) δ: 8.75-8.70 (m, 1H), 8.44-8.39 (m, 1H), 7.70-7.44 (m, 4H), 7.13-7.07 (m, 2H), 2.20 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139589B2
Source datasetuspto-grants-2015_09
ORD IDord-6973f4ef799946c28cf3d1a7f2939532
Source noteuspto-grants-2015_09