Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972693Generated: November 1, 2026

Triethylamine → HCID 86670442, compound

https://huagongshe.com/reaction/1972693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 66584347HCID 66584347—
Reactant2-(2-Chloropyrimidin-5-yl)-1,1,1,3,3,3-hexafluoropropan-2-olHCID 86670348—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86670442HCID 86670442—
ProductHCID 86670443HCID 86670443—

Reaction Conditions

Temperature100 °C

Reaction Steps

In a 50-mL sealed vial, a mixture of (S)-3-(prop-1-yn-1-yl)-1-(thiophen-2-ylsulfonyl)piperazine (40 mg, 0.148 mmol), 2-(2-chloropyrimidin-5-yl)-1,1,1,3,3,3-hexafluoropropan-2-ol (41.5 mg, 0.148 mmol), and triethylamine (30.9 μl, 0.222 mmol) in dioxane was heated to 100° C. for 16 h. Afterwards, the mixture was concentrated and the crude material was purified via column chromatography (about 40 g silica gel, 0% to 10% MeOH in CH2Cl2) to give the racemate of 1,1,1,3,3,3-hexafluoro-2-(2-((2S)-2-(1-propyn-1-yl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)-5-pyrimidinyl)-2-propanol (18 mg) and 1,1,1,3,3,3-hexafluoro-2-(2-((2R)-2-(1-propyn-1-yl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)-5-pyrimidinyl)-2-propanol (18 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-2192ccca44454974a9b66c319d7b37aa
Source noteuspto-grants-2013_04