Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854606Generated: November 2, 2026

4-Methoxybenzylamine → N-(4-Methoxybenzyl)-5-[6-(4-methylpyridin-2-ylamino)pyridin-2-yl]oxazol-2-amine

https://huagongshe.com/reaction/1854606

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzylamineHCID 75452—
Reactant2-Chloro-1,3-oxazoleHCID 13371074—
Reactant5-[6-(4-methylpyridin-2-ylamino)pyridin-2-yl]-N-(pyridin-4-ylmethyl)oxazol-2-amineHCID 67345865—
SolventIsopropanolHCID 3776—
ProductN-(4-Methoxybenzyl)-5-[6-(4-methylpyridin-2-ylamino)pyridin-2-yl]oxazol-2-amineHCID 67324618—

Reaction Steps

Prepared as for 5-[6-(4-methylpyridin-2-ylamino)pyridin-2-yl]-N-(pyridin-4-ylmethyl)oxazol-2-amine above from the chlorooxazole and 4-methoxybenzylamine in iPrOH. 1H NMR (300 MHz, DMSO-d6) δ 9.60 (s, 1H), 8.18-8.00 (m, 2H), 7.75 (s, 1H), 7.63 (t, J=7.9 Hz, 1H), 7.45 (d, J=8.3 Hz, 1H), 7.38-7.24 (m, 3H), 6.95-6.86 (m, 3H), 6.73 (d, J=5.0 Hz, 1H), 4.37 (d, J=5.9 Hz, 2H), 3.72 (s, 3H), 2.30 (s, 3H). (ESI+) m/z 388 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962665B2
Source datasetuspto-grants-2015_02
ORD IDord-d5e62c63b1634d0c9d537571fdc1fb56
Source noteuspto-grants-2015_02