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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712023Generated: November 2, 2026

Triethyloxonium tetrafluoroborate → HCID 178451649, compound

https://huagongshe.com/reaction/712023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
Reactanttert-Butyl 3-carbamoylazetidine-1-carboxylateHCID 21307329—
ReactantHCID 178511084HCID 178511084—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178451649HCID 178451649—

Reaction Steps

A mixture of tert-butyl 3-(aminocarbonyl)azetidine-1-carboxylate (156 mg, 0.779 mmol) and triethyloxonium tetrafluoroborate (280 mg, 1.5 mmol) in tetrahydrofuran (0.4 mL) was stirred at room temperature for 1 h and then concentrated. A mixture of {trans-4-[(6-aminothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}acetonitrile (39 mg, 0.14 mmol) and the above made reagent in ethanol (0.70 mL) was heated at reflux for 2 h. The mixture was cooled to room temperature, diluted with EtOAc, washed with sat. NaHCO3 solution, dried over MgSO4, concentrated and purified on silica gel column (0-5% MeOH in methylene chloride) to give the desired product. LCMS calculated for C24H30N5O2S (M+H)+: m/z=452.2. Found: 452.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181271B2
Source datasetuspto-grants-2015_11
ORD IDord-51ca3e2370e44ed7a9657857feb461c4
Source noteuspto-grants-2015_11