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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048471Generated: November 2, 2026

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

https://huagongshe.com/reaction/2048471

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 numberUS08592431B2
Source datasetuspto-grants-2013_11
ORD IDord-5db451a82f2b465abf1b7c43b1f5bccc
Source noteuspto-grants-2013_11