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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524026Generated: November 4, 2026

4-(2-Bromophenoxy)pyrimidin-2-amine → 4-{[4'-(2-Aminopyrimidin-5-yl)-3'-fluorobiphenyl-2-yl]oxy}pyrimidin-2-amine

https://huagongshe.com/reaction/1524026

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Bromophenoxy)pyrimidin-2-amineHCID 80860076—
Reactant5-(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrimidin-2-amineHCID 90313142—
Product4-{[4'-(2-Aminopyrimidin-5-yl)-3'-fluorobiphenyl-2-yl]oxy}pyrimidin-2-amineHCID 90315183—

Reaction Steps

The title compound was prepared in a manner similar to that described in Example 88 using 4-(2-bromophenoxy)pyrimidin-2-amine and 5-(2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrimidin-2-amine. MS (ESI): mass calcd. for C20H15FN6O, 374.13; m/z found, 375.1 [M+H]+. 1H NMR (500 MHz, CD3OD) δ 8.46 (s, 2H), 7.98-7.94 (d, J=5.8, 1H), 7.53-7.49 (d, J=7.6, 1H), 7.49-7.42 (m, 2H), 7.41-7.36 (m, 1H), 7.36-7.32 (d, J=8.2, 1H), 7.32-7.27 (m, 1H), 7.26-7.14 (d, J=8.0, 1H), 6.13-6.04 (d, J=5.8, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079866B2
Source datasetuspto-grants-2015_07
ORD IDord-c852ba86e838437abc42c92a4330b95c
Source noteuspto-grants-2015_07