Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797137Generated: October 26, 2026

Sodium Acetate → 4-[5-Benzyl-3-(4-chloro-phenyl)-[1,2,4]triazol-1-yl]-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine

https://huagongshe.com/reaction/1797137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant4-Hydrazinyl-6-(pyridin-2-yl)-1,3,5-triazin-2-amineHCID 608952—
ReactantN-(4-chloro-thiobenzoyl)-2-phenyl-acetamideHCID 22174859—
ReactantHOAc dioxaneHCID 22565020—
SolventWaterHCID 962—
Product4-[5-Benzyl-3-(4-chloro-phenyl)-[1,2,4]triazol-1-yl]-6-pyridin-2-yl-[1,3,5]triazin-2-ylamineHCID 2217486860%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of N-(4-chloro-thiobenzoyl)-2-phenyl-acetamide (0.536 g, 1.85 mmol) and sodium acetate (ca. 0.25 g) in 1:1 acetic acid/1,4-dioxane (30 mL) was added 4-hydrazino-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine (0.376 g, 1.85 mmol). The solution was heated to 90° C. and stirred for 15 hours. The reaction mixture was allowed to cool to room temperature, and water (100 mL) was added. The precipitate was removed by filtration, triturated with hot ethanol (300 mL), and dried to provide 0.489 g (60%) of the product as a white solid: 1H NMR (DMSO-d6) δ 8.78 (d, J=4.3 Hz, 1H), 8.32 (d, J=6.1 Hz, 2H), 8.22 (d, J=7.8 Hz, 1H), 8.06 (d, J=8.5 Hz, 2H), 7.96 (dt, J=1.5, 7.8 Hz, 1H), 7.62–7.57 (m, 3H), 7.36–7.26 (m, 2H), 7.24–7.22 (m, 2H), 7.19–7.16 (m, 1H), 4.90 (s, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034031B2
Source datasetuspto-grants-2006_04
ORD IDord-7460869d9e064d709ea3ccfafaf6d52b
Source noteuspto-grants-2006_04