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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523936Generated: November 1, 2026

4-((2-Bromophenyl)sulfonyl)piperazin-2-one → 3-Amino-6-{3-fluoro-2'-[(3-oxopiperazin-1-yl)sulfonyl]biphenyl-4-yl}pyrazine-2-carbonitrile

https://huagongshe.com/reaction/1523936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((2-Bromophenyl)sulfonyl)piperazin-2-oneHCID 7937717—
Reactant3-Amino-6-(2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrazine-2-carbonitrileHCID 90313553—
Product3-Amino-6-{3-fluoro-2'-[(3-oxopiperazin-1-yl)sulfonyl]biphenyl-4-yl}pyrazine-2-carbonitrileHCID 90312864—

Reaction Steps

The title compound was prepared in a manner similar to that described in Example 88 using 4-((2-bromophenyl)sulfonyl)piperazin-2-one and 3-amino-6-(2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrazine-2-carbonitrile. MS (ESI): mass calcd. for C21H17FN6O3S, 452.11; m/z found, 453.0 [M+H]+. 1H NMR (500 MHz, CD3OD) δ 8.65 (d, J=2.1, 1H), 8.05 (dd, J=8.1, 1.3, 1H), 7.85 (m, 1H), 7.65 (m, 1H), 7.55 (m, 1H), 7.36 (dd, J=7.6, 1.3, 1H), 7.26-7.17 (m, 2H), 3.29 (s, 2H), 3.04 (s, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079866B2
Source datasetuspto-grants-2015_07
ORD IDord-214b3676de0a49eda589b17ad2b8de81
Source noteuspto-grants-2015_07