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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1412442Generated: November 2, 2026

N,N,N-Tributylbutan-1-aminium fluoride--hydrogen fluoride (1/1/2) → HCID 178438726, compound

https://huagongshe.com/reaction/1412442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N-Tributylbutan-1-aminium fluoride--hydrogen fluoride (1/1/2)HCID 11748636—
ReactantHCID 178438714HCID 178438714—
SolventChlorobenzeneHCID 7964—
ProductHCID 178438726HCID 17843872652.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3′-fluoro-4′-({4-[trans-4-(1-oxiran-2-ylethoxy)cyclohexyl]-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (0.15 g), tetra-n-butylammonium dihydrogentrifluoride (0.49 g) and chlorobenzene (0.5 mL) was stirred at 120° C. for 24 hr and then at room temperature for 40 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.081 g, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921379B2
Source datasetuspto-grants-2014_12
ORD IDord-8a5f3a86c6d8469fab708a30fb0cf258
Source noteuspto-grants-2014_12