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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424523Generated: November 2, 2026

Methane → N-Cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide

https://huagongshe.com/reaction/1424523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactanttert-Butyl 4-(cyclopropylamino)piperidine-1-carboxylateHCID 2769591—
Reactant4-(1,3-Oxazol-5-yl)benzoic AcidHCID 2776414—
SolventDimethylformamideHCID 6228—
ProductN-Cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamideHCID 68289931—

Reaction Steps

2-(1H-Benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (6.10 g) is added to a solution of 4-oxazol-5-yl-benzoic acid (3.00 g) and ethyldiisopropylamine (5.56 mL) in N,N-dimethylformamide (50 mL) at room temperature. The solution is stirred for 10 min prior to the addition of 4-cyclopropylamino-piperidine-1-carboxylic acid tert-butyl ester (4.57 g). The resulting mixture is kept at room temperature over night. The mixture is treated with activated charcoal and filtered through a pad of basic aluminum oxide. The pad is washed with N,N-dimethylformamide/methanol (9:1) and the combined filtrates are concentrated in vacuo. The residue is dissolved in 1,4-dioxane (35 mL), a 4 M solution of hydrogen chloride in 1,4-dioxane (20 mL) is added and the resulting mixture is stirred at room temperature for 2 h. The solvent is evaporated and the residue is taken up in water. The resulting mixture is washed with dichloromethane, basified with NaOH solution and extracted with dichloromethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927726B2
Source datasetuspto-grants-2015_01
ORD IDord-a4c88af9a14c4343a819cf53c05d3a33
Source noteuspto-grants-2015_01