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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392407Generated: November 3, 2026

Triethylamine → HCID 178522466, compound

https://huagongshe.com/reaction/1392407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 178522467HCID 178522467—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 178522466HCID 17852246643.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To the solution of 4-[N-[1-[N-(benzofuran-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-1-[2-(1H-tetrazol-5-yl)phenyl]piperidin-3-ol (120 mg, 0.22 mmol) obtained in Step 2 in 5 ml of dimethyl sulfoxide (DMSO), was added 0.093 ml of triethylamine (0.66 mmol). The reaction mixture was cooled to 0° C. Pyridine-SO3 complex (103 mg, 0.66 mmol) was added to the reaction mixture, which was then stirred for about 2 hours at room temperature. The reaction mixture was diluted with 100 ml of ethyl acetate, washed with brine. The resulting organic layer was dried on sodium sulfate. The resulting residue was purified with column chromatography to give 50 mg of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07342027B2
Source datasetuspto-grants-2008_03
ORD IDord-43caa6243c514374891d0f1525d84b18
Source noteuspto-grants-2008_03