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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352368Generated: October 26, 2026

1-(5-Trifluoromethyl-thiazol-2-yl)-piperazine hydrochloride → [5-Methanesulfonyl-2-((R)-2,2,2-trifluoro-1-methyl-ethoxy)-phenyl]-[4-(5-trifluoromethyl-thiazol-2-yl)-piperazin-1-yl]-methanone

https://huagongshe.com/reaction/1352368

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Trifluoromethyl-thiazol-2-yl)-piperazine hydrochlorideHCID 21100200—
Reactant5-Methylsulfonyl-2-[((R)-2,2,2-trifluoro-1-methylethyl)oxy]benzoic acidHCID 58863354—
Product[5-Methanesulfonyl-2-((R)-2,2,2-trifluoro-1-methyl-ethoxy)-phenyl]-[4-(5-trifluoromethyl-thiazol-2-yl)-piperazin-1-yl]-methanoneHCID 1157005057%

Reaction Steps

Prepared in analogy to example 1 (b) from 5-methanesulfonyl-2-((R)-2,2,2-trifluoro-1-methyl-ethoxy)-benzoic acid (Example A16) and 1-(5-trifluoromethyl-thiazol-2-yl)-piperazine hydrochloride (Example 58(c)). The crude material was purified by chromatography (SiO2, ethyl acetate/heptane) followed by trituration in pentane to yield the title compound as an off-white crystalline solid (yield 57%). MS (m/e): 532.0 (M+H+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220744B2
Source datasetuspto-grants-2007_05
ORD IDord-1ff627c4cf654f4296b658df5da4392e
Source noteuspto-grants-2007_05