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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177590Generated: October 31, 2026

Sodium Bicarbonate → HCID 86271308, compound

https://huagongshe.com/reaction/2177590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant2-Chloro-3-(trifluoromethyl)benzoyl chlorideHCID 3827633—
ReactantHCID 90409694HCID 90409694—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86271308HCID 8627130882%

Reaction Conditions

Temperature23 °C

Reaction Steps

A suspension of 1-pyrazin-2-yl-1H-[1,2,3]triazolo[4,5-c]pyridine (100 mg, 0.5 mmol) in THF (2.5 mL) was treated with 2-chloro-3-(trifluoromethyl)benzoyl chloride (135 mg, 0.56 mmol) and the reaction stirred for 10 min at 23° C. The reaction was cooled to −50° C. and treated with MeMgBr (3.0 M solution in Et2O, 0.18 mL, 0.56 mmol), and reaction slowly warmed to 23° C. over 30 minutes. Saturated NaHCO3 solution was added to the reaction mixture, which was then extracted with EtOAc and purified on 16 g SiO2 with 0-50% ethyl acetatehexanes to provide 174 mg (82%) of 5-{[2-chloro-3-(trifluoromethyl)phenyl]carbonyl}-4-methyl-1-pyrazin-2-yl-4,5-dihydro-1H-[1,2,3]triazolo[4,5-c]pyridine. MS (ESI): mass calcd. for C18H12ClF3N6O, 420.1. m/z found, 421.1 [M+H]+. 1H NMR (400 MHz, CDCl3) δ 9.64-9.45 (t, J=1.8 Hz, 1H), 8.75-8.58 (d, J=2.6 Hz, 1H), 8.51-8.38 (ddd, J=6.8, 2.6, 1.5 Hz, 1H), 7.95-7.78 (dt, J=4.5, 1.8 Hz, 1H), 7.70-7.38 (m, 2H), 6.69-6.54 (m, 1H), 6.44-6.22 (m, 2H), 1.70-1.50 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09066946B2
Source datasetuspto-grants-2015_06
ORD IDord-ec5bef20cd404b8b9d88f483db2d6128
Source noteuspto-grants-2015_06