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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521654Generated: November 2, 2026

Sodium Carbonate → 7-(5-Fluoropyridin-3-yl)-1-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline-6-carbonitrile

https://huagongshe.com/reaction/1521654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1,4-DioxaneHCID 31275—
Reactant(5-Fluoropyridin-3-yl)boronic acidHCID 44717403—
Reactant7-Bromo-1-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline-6-carbonitrileHCID 70977814—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Product7-(5-Fluoropyridin-3-yl)-1-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline-6-carbonitrileHCID 89961575—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 7-bromo-1-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline-6-carbonitrile (145-4; 0.20 g, 0.0006 mol) and (5-fluoropyridin-3-yl)boronic acid (0.97 g, 0.0006 mol) in the mixture of 1,4-dioxan (10 mL) and water (10 mL) was added sodium carbonate (0.190 g, 0.0018). Reaction mass was purged with argon for 20 min. Then catalyst Pd(dppf)2Cl2 (0.048 g, 0.00006 mol) was added and allowed to stir at 80° C. for 12 h. The reaction mixture was filtered through celite bed and filter bed was thoroughly washed with ethyl acetate. The collected organic part was concentrated under vacuum to afford the crude compound, which was purified by silica gel column chromatography to obtain title compound. 1H NMR (400 MHz, DMSO-d6) δ 8.739-8.732 (d, J=2.8 Hz, 1H), 8.685 (s, 1H), 8.095-8.066 (d, J=11.6 Hz, 2H), 7.782-7.742 (d, J 8 Hz, 1H), 3.282-3.240 (t, J=8.8 Hz, 2H), 3.143-3.109 (t, J=7.6 Hz, 2H), 2.702 (s, 3H). MS (M+1): 306.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073929B2
Source datasetuspto-grants-2015_07
ORD IDord-0212f3a4acbf46c9854be95e5fe1d03c
Source noteuspto-grants-2015_07