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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523893Generated: October 26, 2026

5-(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrimidin-2-amine → 4'-(2-Aminopyrimidin-5-yl)-N-ethyl-3'-fluoro-4-(trifluoromethyl)biphenyl-2-sulfonamide

https://huagongshe.com/reaction/1523893

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrimidin-2-amineHCID 90313142—
Reactant2-Bromo-N-ethyl-5-(trifluoromethyl)benzenesulfonamideHCID 90313690—
Product4'-(2-Aminopyrimidin-5-yl)-N-ethyl-3'-fluoro-4-(trifluoromethyl)biphenyl-2-sulfonamideHCID 90314583—

Reaction Steps

The title compound was prepared in a manner similar to that described in Example 88 using 2-bromo-N-ethyl-5-(trifluoromethyl)benzenesulfonamide 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 C19H16F4N4O2S, 440.09; m/z found, 441.0 [M+H]+. 1H NMR (500 MHz, CD3OD) δ 8.56-8.53 (d, J=1.4, 2H), 8.34-8.31 (m, 1H), 7.99-7.95 (m, 1H), 7.63-7.59 (d, J=8.0, 1H), 7.59-7.53 (m, 1H), 7.36-7.34 (dd, J=7.1, 1.6, 1H), 7.34-7.32 (m, 1H), 2.97-2.71 (q, J=7.2, 2H), 1.15-0.84 (t, J=7.2, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079866B2
Source datasetuspto-grants-2015_07
ORD IDord-69ab5d2bff8a4560a12714fb51e52fd4
Source noteuspto-grants-2015_07