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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621535Generated: November 2, 2026

Ammonia → 4-(2-(4-Fluorophenyl)-4-(6-methoxypyridin-3-ylamino)pyrimidin-5-YL)-6-methyl-1,3,5-triazin-2-amine

https://huagongshe.com/reaction/1621535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-(4-fluorophenyl)-N-(6-methoxypyridin-3-yl)-5-(4-methyl-6-(methylthio)-1,3,5-triazin-2-yl)pyrimidin-4-amineHCID 66599856—
Solvent1,4-DioxaneHCID 31275—
Product4-(2-(4-Fluorophenyl)-4-(6-methoxypyridin-3-ylamino)pyrimidin-5-YL)-6-methyl-1,3,5-triazin-2-amineHCID 59548430—

Reaction Conditions

Temperature100 °C

Reaction Steps

A glass microwave reaction vessel was charged with 2-(4-fluorophenyl)-N-(6-methoxypyridin-3-yl)-5-(4-methyl-6-(methylthio)-1,3,5-triazin-2-yl)pyrimidin-4-amine (12 mg, 0.028 mmol), ammonia (0.5 mL, 30% in water) and dioxane (1 mL). The reaction mixture was stirred and heated in a oil bath at 100° C. for 17 h. The solvent was removed in vacuo and the residue was purified by silica gel chromatography eluting with 80% EtOAc/hexanes to give 4-(2-(4-fluorophenyl)-4-(6-methoxypyridin-3-ylamino)pyrimidin-5-yl)-6-methyl-1,3,5-triazin-2-amine. 1H NMR (300 MHz, CDCl3) δ 9.60 (s, 1H); 8.35-8.54 (m, 3H); 8.12 (dd, J=8.84, 2.41 Hz, 1H); 7.15 (t, J=8.62 Hz, 2H); 6.86 (d, J=8.92 Hz, 1H); 5.44 (s, 2H); 3.99 (s, 3H); 2.56 (s, 3H). m/z (ESI, +ve ion) 405.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772480B2
Source datasetuspto-grants-2014_07
ORD IDord-3a9b028804f3414cb525faef4704268d
Source noteuspto-grants-2014_07