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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850282Generated: October 30, 2026

Triethylamine → HCID 58547336, compound

https://huagongshe.com/reaction/1850282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-PiperidinemethanolHCID 420771—
ReactantHCID 58546726HCID 58546726—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 58547336HCID 5854733667%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-(3-bromo-5-fluoro-pyridin-2-yl)-azetidine-1-carboxylic acid tert-butyl ester (58) (660 mg, 2 mmol, Preparation 17) and piperidin-4-yl-methanol (35) (230 mg, 2 mmol) in DMSO (20 mL) was added Et3N (404 mg, 4 mmol). The reaction mixture was stirred at 100° C. overnight. The reaction mixture was diluted with water, extracted with EtOAc (50 mL×3). The combined organic extracts were washed with water (30 mL) and brine (30 mL), dried over Na2SO4 and filtered. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography (EtOAc:PE=3:1) on silica gel to give (76) (490 mg, 1.34 mmol, yield 67%). ESI-MS (M+1): 366 calc. for C19H28FN3O3 365.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957073B2
Source datasetuspto-grants-2015_02
ORD IDord-1d84d25cdfbc4b26b45a286ba04eb2e0
Source noteuspto-grants-2015_02