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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621739Generated: October 29, 2026

Ammonia → 4-(Amino(5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-YL)-6-(6-methoxypyridin-3-ylamino)pyridin-3-YL)methyl)-N,N-dimethylbenzenesulfonamide

https://huagongshe.com/reaction/1621739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 86647059HCID 86647059—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product4-(Amino(5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-YL)-6-(6-methoxypyridin-3-ylamino)pyridin-3-YL)methyl)-N,N-dimethylbenzenesulfonamideHCID 66611676—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of (5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-(6-methoxypyridin-3-ylamino)pyridin-3-yl)(4-(N,N-dimethylsulfamoyl)phenyl)methyl methanesulfonate (14.22 mg, 0.017 mmol) in DCM (0.1 mL) was treated with 0.5 M NH3 in dioxane (2 mL). The mixture was allowed to stand overnight, after which time partial conversion to the amine was observed by LCMS. The mixture was then sealed and heated and 80° C. for 2 h, after which time the starting material was consumed. The mixture was concentrated and taken on directly to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772480B2
Source datasetuspto-grants-2014_07
ORD IDord-7b3accae06754d61aac89f030d5ed19c
Source noteuspto-grants-2014_07