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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846789Generated: November 1, 2026

Dimethylformamide → 3-[5-Fluoro-3-(tetrahydro-pyran-4-YL)-pyridin-2-yloxy]-cyclobutanecarboxylic acid methoxy-methyl-amide

https://huagongshe.com/reaction/1846789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant3-[5-Fluoro-3-(tetrahydro-pyran-4-yl)-pyridin-2-yloxy]-cyclobutanecarboxylic acidHCID 58548664—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product3-[5-Fluoro-3-(tetrahydro-pyran-4-YL)-pyridin-2-yloxy]-cyclobutanecarboxylic acid methoxy-methyl-amideHCID 58548567—

Reaction Steps

To a solution of 3-[5-fluoro-3-(tetrahydro-pyran-4-yl)-pyridin-2-yloxy]-cyclobutanecarboxylic acid (1.5 g, 4.68 mmol) was added DMF (20 mL), triethylamine (1 mL, 7.02 mmol), and 2-(1H-benzo[d][1,2,3]triazol-1-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate(V) (2.24 g, 5.90 mmol). The reaction mixture was stirred at RT for 1d. Then it was diluted with water and EtOAc. The organic layer was separated and the aqueous phase was extracted with EtOAc (2×10 mL). All the organic layers were combined and washed with brine (1×10 mL), dried over MgSO4, filtered, and concentrated to get a crude, which was purified by flash column chromatography on silica gel (30% to 70% EtOAc in hexanes) to give the product (2.2 g) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952037B2
Source datasetuspto-grants-2015_02
ORD IDord-142f47cf0368442e91b6656311468350
Source noteuspto-grants-2015_02