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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983450Generated: October 30, 2026

Ammonia → 3-[3-(4-Amino-[1,3,5]triazin-2-yl)-pyridin-2-ylamino]-N-(4-phenoxy-phenyl)benzamide

https://huagongshe.com/reaction/983450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4-(2-chloropyridin-3-yl)-N-(3,4,5-trimethoxyphenyl)-1,3,5-triazin-2-amineHCID 16109005—
Reactant3-Amino-N-(4-phenoxyphenyl)benzamideHCID 22560095—
SolventDimethyl SulfoxideHCID 679—
Product3-[3-(4-Amino-[1,3,5]triazin-2-yl)-pyridin-2-ylamino]-N-(4-phenoxy-phenyl)benzamideHCID 10162549—

Reaction Steps

[4-(2-Chloro-pyridin-3-yl)-[1,3,5]triazin-2-yl]-(3,4,5-trimethoxy-phenyl)amine (Example 2, Step 4) (247 mg, 1.08 mmol) was suspended in a 2 M solution of NH3 in IpOH (3 ml)(Aldrich), and the reaction mixture was stirred overnight in a sealed tube. Concentration, trituration in a small amount of MeOH, and filtration provided a white solid. A portion of this material (97 mg, 0.47 mmol) was mixed with 3-amino-N-(4-phenoxyphenyl)benzamide (320 mg, 0.96 mmol) and DMSO (250 ml), and stirred overnight at 90° C. The dark residue was diluted with IpOH, sonicated, triturated, and then concentrated. Upon dilution with IpOH, a light green solid was isolated by filtration. MS m/z=476.5. [M+H]+. Calc'd for C27H21N7O2: 475.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864255B2
Source datasetuspto-grants-2005_03
ORD IDord-81e7ecd6542446169c6890c6ef5cc728
Source noteuspto-grants-2005_03