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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363326Generated: October 29, 2026

Potassium Carbonate → HCID 66929381, compound

https://huagongshe.com/reaction/1363326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBromoacetonitrileHCID 11534—
ReactantHCID 16051513HCID 16051513—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 66929381HCID 66929381—

Reaction Conditions

Temperature75 °C

Reaction Steps

Alternatively, to a solution of 5-amino-3-[3-(hydroxy)phenylamino]-1-(3-(methyl)phenyl)carbonyl-1H-1,2,4-triazole (Ia-7) (0.84 g, 2.7 mmol) in 2-butanone (9 mL) was added K2CO3 (0.41 g, 3.0 mmol) and BrCH2CN (0.36 g, 3.0 mmol). After stirring the mixture at 75° C. for 20 h, the 2-butanone was removed under reduced pressure. The residue was dissolved in EtOAc (50 mL), washed with water (50 mL), brine (30 mL), dried (Na2SO4) and concentrated to afford the crude product: Recrystallization from CH3CN afforded 5-amino-3-[3-(cyanomethoxy)phenylamino]-1-(3-(methyl)phenyl)carbonyl-1H-1,2,4-triazole (Ia-9) (0.12 g, 13%) as a white solid: Rf 0.22 (1:1 hexanes/ethyl acetate); mp (DSC) 220.0-224.4° C.; 1H NMR (300 MHz, DMSO-d6) δ 9.45 (s, 1H), 8.05 (s, 1H), 7.91 (d, J=7.1 Hz, 1H), 7.83 (s, 2H), 7.50-7.39 (m, 3H), 7.20 (t, J=8.1 Hz, 1H), 7.12-7.09 (m, 1H), 6.56 (dd, J=7.9, 2.2 Hz, 1H), 5.04 (s, 2H), 2.43 (s, 3H); 13C NMR (75 MHz, DMSO-d6) δ 166.6, 157.9, 157.2, 156.9, 142.3, 137.2, 133.0, 132.6, 130.8, 129.5, 127.8, 127.4, 116.5, 111.1, 105.2, 104.0, 53.3, 20.8; IR (ATR) 3449, 3367, 2325, 1684 cm−1; APCI MS m/z 349 [C18H16N6O2+H]+; HPLC (Method A) 96.8% (AUC), tR=12.81 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884119B2
Source datasetuspto-grants-2011_02
ORD IDord-4242c6fd5ca44a33993648f1345e6987
Source noteuspto-grants-2011_02