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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1812175Generated: October 31, 2026

5-Fluoro-6-methoxypyridin-3-amine → 5-(4-Amino-6-methyl-1,3,5-triazin-2-YL)-N-(5-fluoro-6-methoxypyridin-3-YL)-2,3'-bipyridin-6-amine

https://huagongshe.com/reaction/1812175

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-6-methoxypyridin-3-amineHCID 45480351—
Reactant4-(6-fluoro-2,3'-bipyridin-5-yl)-N,N-bis(4-methoxybenzyl)-6-methyl-1,3,5-triazin-2-amineHCID 66611426—
Product5-(4-Amino-6-methyl-1,3,5-triazin-2-YL)-N-(5-fluoro-6-methoxypyridin-3-YL)-2,3'-bipyridin-6-amineHCID 59548385—

Reaction Steps

The title compound was prepared in an analogous manner to that described in Example 254 using 4-(6-fluoro-2,3′-bipyridin-5-yl)-N,N-bis(4-methoxybenzyl)-6-methyl-1,3,5-triazin-2-amine and 5-fluoro-6-methoxypyridin-3-amine (Anichem), and was isolated as an orange amorphous solid (5.7%). m/z (ESI, +ve ion) 405.0 (M+H)+. 1H NMR (400 MHz, d6-DMSO) δ 12.03 (1H, s); 9.27 (1H, d, J=2.0 Hz); 8.91 (1H, d, J=8.2 Hz); 8.67 (1H, dd, J=4.8, 1.5 Hz); 8.55 (1H, d, J=2.2 Hz); 8.39-8.43 (1H, m); 8.36 (1H, dd, J=12.7, 2.3 Hz); 7.93 (1H, br. s.); 7.79 (1H, br. s.); 7.62 (1H, d, J=8.2 Hz); 7.57 (1H, dd, J=7.9, 4.8 Hz); 3.96 (3H, s); 2.45 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362241B2
Source datasetuspto-grants-2013_01
ORD IDord-19150d0a1f9646a3b47d472a6c84b0c0
Source noteuspto-grants-2013_01