Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838203Generated: November 2, 2026

1-(4-Fluorophenyl)piperazine → HCID 86587515, compound

https://huagongshe.com/reaction/1838203

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86587516HCID 86587516—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86587515HCID 86587515—

Reaction Steps

In analogy to the procedure described in example 20b, 2-amino-4-bromo-6-methyl-sulfanyl-pyrimidine-5-carbonitrile (see example 69) was treated with 1-(4-fluorophenyl)-piperazine in dioxane in the presence of N-ethyl-diisopropylamine at room temperature during 36 hours to yield 2-amino-4-[4-(4-fluoro-phenyl)-piperazin-1-yl]-6-methyl-sulfanyl-pyrimidine-5-carbonitrile as a yellow powder; MS: [M+H]+=345.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673795B2
Source datasetuspto-grants-2004_01
ORD IDord-6a2c606b7a3f4bef8a1c9ba55971a7cf
Source noteuspto-grants-2004_01