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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234378Generated: October 31, 2026

Diisopropylethylamine → 2-Fluoro-N-(1-methyl-4-piperidinyl)-4-nitrobenzamide

https://huagongshe.com/reaction/2234378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Fluoro-4-nitrobenzoic acidHCID 302679—
Reactant4-Amino-1-methylpiperidineHCID 2737531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
Product2-Fluoro-N-(1-methyl-4-piperidinyl)-4-nitrobenzamideHCID 5800976959%

Reaction Steps

2-Fluoro-4-nitrobenzoic acid (Aldrich; 3 g, 16.21 mmol), 4-Amino-1-methylpiperidine (Fluorochem; 2.03 g, 17.83 mmol), HATU (6.77 g, 17.83 mmol), DIPEA (8.5 mL, 48.63 mmol) and DMF (30 mL) were combined and stirred at ambient temperature for 18 hrs. Solvents evaporated and partitioned between DCM (200 ml) and water (100 ml). The aqueous phase was re-extracted with DCM (100 ml). The combined organic phases were dried (MgSO4) and evaporated. The resultant material was taken up in DCM and purified on silica eluting with a gradient of 0-5% 2M ammonia in MeOH/DCM then 5% 2M ammonia in MeOH/DCM. Fractions containing product were combined and evaporated to give the title compound as a yellow solid (2.67 g, 59%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709471B2
Source datasetuspto-grants-2010_05
ORD IDord-a4ecb489d4a1426eb37782a8decd4505
Source noteuspto-grants-2010_05