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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1812147Generated: October 30, 2026

Trifluoroacetic acid → 4-(amino(5-(4-amino-6-methyl-1,3,5-triazin-2-yl)-6-(6-methoxypyridin-3-ylamino)pyridin-3-yl)methyl)-N,N-dimethylbenzenesulfonamide trifluoroacetate

https://huagongshe.com/reaction/1812147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(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—
Product4-(amino(5-(4-amino-6-methyl-1,3,5-triazin-2-yl)-6-(6-methoxypyridin-3-ylamino)pyridin-3-yl)methyl)-N,N-dimethylbenzenesulfonamide trifluoroacetateHCID 66611612—

Reaction Steps

A solution of 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 (12.88 mg, 0.017 mmol) in TFA (1 mL) was heated at 100° C. in a sealed tube for 4 h, after which time reaction was complete. The mixture was concentrated and purified by prep HPLC to give 4-(amino(5-(4-amino-6-methyl-1,3,5-triazin-2-yl)-6-(6-methoxypyridin-3-ylamino)pyridin-3-yl)methyl)-N,N-dimethylbenzenesulfonamide trifluoroacetate (3.2 mg). m/z (ESI, +ve ion) 522 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362241B2
Source datasetuspto-grants-2013_01
ORD IDord-c6c1c1c5d3df450498f2f09d5841a22c
Source noteuspto-grants-2013_01