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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713772Generated: November 1, 2026

6-Chloronicotinamide → 6-{4-[({5-[(2-Fluorophenyl)amino]-1,3,4-oxadiazol-2-yl}carbonyl)amino]-piperidin-1-yl}nicotinamide

https://huagongshe.com/reaction/1713772

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-ChloronicotinamideHCID 80456—
Reactant5-[(2-fluorophenyl)amino]-N-piperidin-4-yl-1,3,4-oxadiazole-2-carboxamideHCID 59464130—
SolventDimethylformamideHCID 6228—
Product6-{4-[({5-[(2-Fluorophenyl)amino]-1,3,4-oxadiazol-2-yl}carbonyl)amino]-piperidin-1-yl}nicotinamideHCID 594642832.5%

Reaction Steps

A solution of 5-[(2-fluorophenyl)amino]-N-piperidin-4-yl-1,3,4-oxadiazole-2-carboxamide (Intermediate 101) (200 mg, 0.66 mmol) and 6-chloronicotinamide (103 mg, 0.66 mmol) in dry DMF (4 mL) was heated in the microwave at 125° C. for 20 minutes and then for a further 10 minutes at 135° C. The mixture was filtered and purified by preparative HPLC to give the title compound (7 mg, 2.5%) as a solid; 1H NMR δ 1.55-1.65 (2H, m), 1.83-1.86 (2H, m), 2.99 (2H, t), 4.04-4.12 (1H, m), 4.42-4.46 (2H, m), 6.87 (1H, d), 7.11 (2H, m), 7.21-7.30 (2H, m), 7.72 (1H, s), 7.94-8.03 (2H, m), 8.62 (1H, d), 8.99 (1H, d), 10.61 (1H, s); MS m/e MH+ 426.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795283B2
Source datasetuspto-grants-2010_09
ORD IDord-f8788030854442fda00208ad04405e12
Source noteuspto-grants-2010_09