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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282278Generated: November 1, 2026

Dimethylformamide → 4-bromo-2-(2-methylpyrazolo[1,5-a]pyridin-3-yl)-5-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-1,2,4-triazol-3-yl)thiazole

https://huagongshe.com/reaction/2282278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantPyridinium, 1-amino-, iodide (1:1)HCID 2733704—
Reactant3-(4-bromo-2-prop-1-yn-1-yl-1,3-thiazol-5-yl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-1,2,4-triazoleHCID 58094952—
Product4-bromo-2-(2-methylpyrazolo[1,5-a]pyridin-3-yl)-5-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-1,2,4-triazol-3-yl)thiazoleHCID 5809485264.8%

Reaction Steps

A mixture of 3-(4-bromo-2-prop-1-yn-1-yl-1,3-thiazol-5-yl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-1,2,4-triazole (0.514 g, 1.29 mmol), 1-Aminopyridinium iodide (0.343 g, 1.54 mmol) and Potassium carbonate (0.231 g, 1.67 mmol) in N,N-Dimethylformamide (8.0 mL, 1.0E2 mmol) was stirred at r.t. for 29 hours. The mixture was quenched with ice water (80 mL), extracted with EtOAc 3 times. The combined EtOAc solution was washed with water, brine, dried over Na2SO4, filtered and EtOAc/hexane (0/100 to 30/70) to afford a solid product. (0.410 g, 64.8% yield). LCMS: (FA) ES+491, 493. 1H NMR (400 MHz, d1-chloroform) δ 8.43-8.46 (m, 2H), 8.32 (s, 1H), 7.39-7.42 (m, 1H), 6.90-6.93 (m, 1H), 5.57 (s, 2H), 3.72-3.76 (m, 2H), 2.76 (s, 3H), 0.96-1.00 (m, 2H), 0.00 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139589B2
Source datasetuspto-grants-2015_09
ORD IDord-d820286888be428198da749045c87e78
Source noteuspto-grants-2015_09