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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993667Generated: October 30, 2026

Triethylamine → HCID 68536996, compound

https://huagongshe.com/reaction/1993667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,6-Difluorobenzoyl chlorideHCID 87438—
ReactantHCID 68538445HCID 68538445—
SolventDichloromethaneHCID 6344—
ProductHCID 68536996HCID 6853699691%

Reaction Steps

Add triethylamine (2.57 mL, 18.5 mmol) to a suspension of 1.1 g (3.7 mmol) of 4-nitro-2-(piperidin-4-yloxy)-pyridine dihydrochloride in dry dichloromethane (50 mL). Then add 2,6-difluorobenzoyl chloride, 0.512 mL (4.07 mmol). Stir the mixture at room temperature overnight. Add water (50 mL) and separate organic layer. Dry with MgSO4 and filter. Evaporate solvents to obtain 1.22 g (91% yield) of (2,6-difluoro-phenyl)-[4-(4-nitro-pyridin-2-yloxy)-piperidin-1-yl]-methanone as a yellow solid (ES+(m/z)=364 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652015B2
Source datasetuspto-grants-2010_01
ORD IDord-37396d23fd6d4733bf4e7855bdbd753b
Source noteuspto-grants-2010_01