Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517990Generated: November 1, 2026

N-methyl-2-pyrrolidone → 6-(4-(3-(4-hydroxy-4-methylpiperidin-1-yl)propoxy)-3-(trifluoromethyl)phenyl)-1-methyl-1H-[1,2,3]triazolo[4,5-d]pyridine-4-carbonitrile

https://huagongshe.com/reaction/517990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant4-Methylpiperidin-4-ol hydrochlorideHCID 21949295—
Reactant3-(4-(4-cyano-1-methyl-1H-benzo[d][1,2,3]triazol-6-yl)-2-(trifluoromethyl)phenoxy)propyl methanesulfonateHCID 86673353—
Product6-(4-(3-(4-hydroxy-4-methylpiperidin-1-yl)propoxy)-3-(trifluoromethyl)phenyl)-1-methyl-1H-[1,2,3]triazolo[4,5-d]pyridine-4-carbonitrileHCID 53330393—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-(4-(4-cyano-1-methyl-1H-benzo[d][1,2,3]triazol-6-yl)-2-(trifluoromethyl)phenoxy)propyl methanesulfonate (100 mg) and 4-methylpiperidin-4-ol hydrochloride (166 mg) in NMP (2 ml) was heated at 100° C. under microwave conditions for 30 minutes. The mixture was purified by HPLC to give the expected product (9.4 mg). 1H NMR (CD3OD) δ: 8.55 (s, 1H), 8.35-8.42 (m, 2H), 7.32 (d, 1H), 4.44 (s, 3H), 4.25 (t, 2H), 2.76-2.89 (m, 4H), 2.63-2.75 (m, 2H), 2.13 (quin, 2H), 1.64-1.80 (m, 4H), 1.24 (s, 3H). MS m/z 475 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115126B2
Source datasetuspto-grants-2015_08
ORD IDord-b364fc6e328d4fa3b2a83d20ac2df108
Source noteuspto-grants-2015_08