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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472365Generated: October 29, 2026

1-(4-Bromophenyl)-4-methylpiperazine → HCID 57502391, compound

https://huagongshe.com/reaction/472365

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromophenyl)-4-methylpiperazineHCID 11817675—
ReactantHCID 67478912HCID 67478912—
ProductHCID 57502391HCID 57502391—

Reaction Steps

[6-Fluoro-8-(4-methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[4-(4-methyl-piperazin-1-yl)-phenyl]-amine was prepared from 6-fluoro-8-(4-methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine and 1-(4-bromo-phenyl)-4-methyl-piperazine in a manner analogous to Step 2d and was isolated as an orange solid (23% yield). 1H NMR (400 MHz, CDCl3, δ, ppm): 8.45 (s, 1H), 8.26 (d, J=8.0 Hz, 2H), 8.11 (d, J=7.7 Hz, 2H), 7.58 (d, J=9.0 Hz, 1H), 7.48 (dd, J=11.5 Hz, 7.8 Hz, 2H), 6.98 (d, J=7.9 Hz, 2H), 6.76 (s, 1H), 3.27 (bm, 4H), 3.12 (s, 3H), 2.62 (bm, 4H), 2.38 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633173B2
Source datasetuspto-grants-2014_01
ORD IDord-8872798a33d44ca896d866dd3c960c25
Source noteuspto-grants-2014_01