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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882216Generated: November 1, 2026

3-Bromo-5-chloropyridin-2-amine → 3-(3-Bromo-5-chloro-pyridin-2-ylamino)-5-chloro-1-(4-methoxy-benzyl)-1H-pyrazin-2-one

https://huagongshe.com/reaction/1882216

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-5-chloropyridin-2-amineHCID 2763971—
Reactant1-(4-methoxybenzyl)-3,5-dichloropyrazine-2(1H)-oneHCID 15498463—
Product3-(3-Bromo-5-chloro-pyridin-2-ylamino)-5-chloro-1-(4-methoxy-benzyl)-1H-pyrazin-2-oneHCID 1612354558%

Reaction Steps

The title compound was prepared in 58% yield from 2-amino-3-bromo-5-chloropyridine and 3,5-dichloro-1-(4-methoxy-benzyl)-1H-pyrazin-2-one in a manner analogous to that for the preparation of example 26. 1H NMR (400 MHz, DMSO-d6): δ 9.58 (s, 1H), 8.51 (d, 1H, J=2.4 Hz), 8.40 (d, 1H, J=2.4 Hz), 7.51 (s, 1H), 7.36 (d, 2H, J=8.8 Hz), 6.92 (d, 2H, J=8.8 Hz), 5.00 (s, 2H), 3.73 (s, 3H). MS (ES) [m+H] calc'd for C17H13BrCl2N4O2, 455, 457, 459; found 455, 457, 459.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318939B2
Source datasetuspto-grants-2012_11
ORD IDord-9f703f0f57ff4f49a56bbe1cfa9bbbb9
Source noteuspto-grants-2012_11